Explore numerous industrial engineering jobs that focus on optimizing complex systems and processes. These roles demand analytical minds capable of improving efficiency and productivity across various sectors. Industrial engineers are vital in manufacturing, logistics, and supply chain management, applying principles of engineering, mathematics, and business to streamline operations.223 Industrial Engineering jobs in Ireland
Manufacturing Engineering Team Lead
Limerick, Munster
J&J Family of Companies
Posted today
Job Viewed
Job Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
Supply Chain Manufacturing
**Job Sub** **Function:**
Production Equipment Repair & Maintenance
**Job Category:**
People Leader
**All Job Posting Locations:**
Limerick, Ireland
**Job Description:**
**About MedTech**
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at are searching for the best talent for the Manufacturing Engineering Team Lead (METL) roles to be in Limerick.**
**Purpose:**
The Manufacturing Engineering Team Lead (METL) supports Operations Management in the production of contact lenses in the Value Stream. Working closely with Engineering, Quality and Operations Line management the role will have direct responsibility for managing key areas of the Value Stream to lead the production of a range of Medical Devices to fulfil global planning schedules, within determined quality and safety standards.
**As a** **Manufacturing Engineering Team Lead, y** **ou will** **:**
+ Lead the Production Unit in close cooperation with Quality and Engineering, to manufacture Medical Devices according to global planning requirements.
+ Ensure all Safety and Quality Standards are upheld top the highest possible standard.
+ Lead year on year efficiency improvement and activity reduction.
+ Build and maintain an environment of innovative continuous improvement, focusing on quality, cost reduction, process development and supply.
+ Lead & mentor supervisory and operations personnel and developing people at all levels to grow within and beyond their current role.
+ Lead specific projects for the Production Unit and across the full Operations function where relevant.
+ Report on achievement of key performance metrics.
+ Support all functions in the effective transfer of new products and processes into manufacturing processes.
+ Ensure that housekeeping standards are maintained at all times across the Value Stream - always looking for opportunities to improve the standard.
**Essential Requirements:**
+ A QQI Level 7 and above in Management or Technical qualification or related discipline
+ Relevant experience in a similar supervisory role
+ Ability to demonstrate standards of leadership - Managing Complexity, Innovations, Customer Focus
+ Technical or people/team management qualification
+ Project Management Skills / Experience with Lean Manufacturing processes/Six Sigma
**Desirable:**
+ Flexible
+ Team focused
+ Good Influencing Skills at all levels (supervisor/direct report)
+ Excellent Communication Skills
+ Technical Knowledge
+ Methodical
At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.
**Here's what you can expect:**
+ **Application review:** We'll carefully review your CV to see how your skills and experience align with the role.
+ **Getting to know you:** If there's a good match, you'll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
+ **Staying informed:** We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
+ **Final steps:** For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.
Finally, at the end of the process, we'll invite you to share feedback in a short survey - your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We're excited to learn more about you and wish you the best of luck in the process! #RPOEMEA
#LI-Onsite
Supply Chain Manufacturing
**Job Sub** **Function:**
Production Equipment Repair & Maintenance
**Job Category:**
People Leader
**All Job Posting Locations:**
Limerick, Ireland
**Job Description:**
**About MedTech**
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at are searching for the best talent for the Manufacturing Engineering Team Lead (METL) roles to be in Limerick.**
**Purpose:**
The Manufacturing Engineering Team Lead (METL) supports Operations Management in the production of contact lenses in the Value Stream. Working closely with Engineering, Quality and Operations Line management the role will have direct responsibility for managing key areas of the Value Stream to lead the production of a range of Medical Devices to fulfil global planning schedules, within determined quality and safety standards.
**As a** **Manufacturing Engineering Team Lead, y** **ou will** **:**
+ Lead the Production Unit in close cooperation with Quality and Engineering, to manufacture Medical Devices according to global planning requirements.
+ Ensure all Safety and Quality Standards are upheld top the highest possible standard.
+ Lead year on year efficiency improvement and activity reduction.
+ Build and maintain an environment of innovative continuous improvement, focusing on quality, cost reduction, process development and supply.
+ Lead & mentor supervisory and operations personnel and developing people at all levels to grow within and beyond their current role.
+ Lead specific projects for the Production Unit and across the full Operations function where relevant.
+ Report on achievement of key performance metrics.
+ Support all functions in the effective transfer of new products and processes into manufacturing processes.
+ Ensure that housekeeping standards are maintained at all times across the Value Stream - always looking for opportunities to improve the standard.
**Essential Requirements:**
+ A QQI Level 7 and above in Management or Technical qualification or related discipline
+ Relevant experience in a similar supervisory role
+ Ability to demonstrate standards of leadership - Managing Complexity, Innovations, Customer Focus
+ Technical or people/team management qualification
+ Project Management Skills / Experience with Lean Manufacturing processes/Six Sigma
**Desirable:**
+ Flexible
+ Team focused
+ Good Influencing Skills at all levels (supervisor/direct report)
+ Excellent Communication Skills
+ Technical Knowledge
+ Methodical
At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.
**Here's what you can expect:**
+ **Application review:** We'll carefully review your CV to see how your skills and experience align with the role.
+ **Getting to know you:** If there's a good match, you'll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
+ **Staying informed:** We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
+ **Final steps:** For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.
Finally, at the end of the process, we'll invite you to share feedback in a short survey - your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We're excited to learn more about you and wish you the best of luck in the process! #RPOEMEA
#LI-Onsite
This advertiser has chosen not to accept applicants from your region.
0
Automation Engineer ( FTC 30.04.2027)
Dublin, Leinster
Takeda Pharmaceuticals
Posted 2 days ago
Job Viewed
Job Description
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
**Automation Engineer**
This position is a **fixed-term role until 30 April 2027** .
At Takeda Grange Castle, our Automation Engineers play a vital role in operating and improving complex manufacturing systems while also supporting and training personnel. Responsibilities vary depending on the assignment, but the Automation Engineer will primarily work with multiple automation systems (PLC/SCADA/DCS) and supporting infrastructure.
This position requires both independent initiative and effective teamwork. The Automation Engineer supports daily operations, contributes to manufacturing goals, and ensures all work meets quality, safety, and environmental standards.
**Key Responsibilities :**
**Daily Operations & System Support**
+ Provide hands-on support for site activities related to PLC/SCADA/DCS systems.
+ Troubleshoot and resolve automation issues in collaboration with Manufacturing, Engineering, and EHS teams.
+ Implement code modifications as needed.
+ Provide accurate updates on task and project progress.
+ Support testing, debugging, and documentation for control system installations.
+ Assist in integrating control systems with data historians (e.g., PI) and MES.
+ Manage system backups and user accounts.
+ Contribute to Data Integrity and compliance programs.
**Project & Technical Support**
+ Collaborate with project teams and departments to develop and troubleshoot automation solutions.
+ Provide technical support for feasibility studies and field trials.
+ Support all stages of qualification (e.g., writing and executing test scripts, working with validation teams).
+ Participate in the rollout of new processes, including recipe development.
**Documentation & Training**
+ Develop and maintain SOPs for site control systems.
+ Create and deliver training for identified users to ensure proper system usage.
+ Cross-train team members to build department-wide automation knowledge.
+ Ensure proper documentation of activities, including SOP logs, EHS records, and logbooks.
**Compliance & Quality**
+ Ensure all activities comply with Takeda's quality standards, cGMP, EHS policies, and regulatory requirements.
+ Prepare reports related to deviations, investigations, and system changes.
+ Support internal audits and inspections where relevant.
**General Expectations**
+ Participate in ongoing training and development.
+ Uphold Takeda-ism values in daily work.
+ Foster a strong safety culture in collaboration with colleagues.
+ Respond to on-call or call-out situations as required.
+ Complete all required SOP readings, training, and assessments.
+ Perform other tasks as directed by the Director of Engineering or other designated leadership.
**What You Bring to Takeda**
+ Degree in Automation, Electrical, or related Engineering discipline.
+ 2-5 years of experience with automation/control systems.
+ Familiarity with Distributed Control Systems (DCS), especially Yokogawa Centum VP, is a plus.
+ Knowledge of Simatic S7 and TIA Portal is desirable.
+ Experience with Wonderware and PI Data Historian is advantageous.
+ Ability to develop IT/automation documentation and SOPs.
+ Strong project management and control system implementation skills.
**What you can look forward to with us:**
+ Competitive Salary: Including performance-based bonuses.
+ Retirement Plan: Employer contributions to your retirement plan.
+ Comprehensive Insurance: Employer-funded private medical insurance with dependants' cover, life insurance, and flexible options like dental insurance, partner life insurance, and serious illness protection.
+ Electric Charging Points: Available at parking locations.
+ Employee Assistance Program: Support for personal and professional challenges.
+ Wellbeing and Engagement: Dedicated teams to support your wellbeing.
+ Family-Friendly Policies: Supportive policies for a balanced work-life.
+ Generous Vacation: 26 vacation days plus additional days for service milestones and humanitarian volunteering leave.
+ Development Opportunities: Coaching, mentoring, educational programs, and formal training.
+ Subsidized Canteen: Enjoy meals at a reduced cost.
+ Flexible Benefits: Options like fuel card, bike to work, commuter ticket, and insurance deals.
**More about us:**
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
**Empowering our people to shine:**
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
If you are interested in this opportunity, we look forward to receiving your application via our online tool!
**Locations**
Grange Castle, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Fixed Term (Fixed Term)
**Time Type**
Full time
**Job Description**
**Automation Engineer**
This position is a **fixed-term role until 30 April 2027** .
At Takeda Grange Castle, our Automation Engineers play a vital role in operating and improving complex manufacturing systems while also supporting and training personnel. Responsibilities vary depending on the assignment, but the Automation Engineer will primarily work with multiple automation systems (PLC/SCADA/DCS) and supporting infrastructure.
This position requires both independent initiative and effective teamwork. The Automation Engineer supports daily operations, contributes to manufacturing goals, and ensures all work meets quality, safety, and environmental standards.
**Key Responsibilities :**
**Daily Operations & System Support**
+ Provide hands-on support for site activities related to PLC/SCADA/DCS systems.
+ Troubleshoot and resolve automation issues in collaboration with Manufacturing, Engineering, and EHS teams.
+ Implement code modifications as needed.
+ Provide accurate updates on task and project progress.
+ Support testing, debugging, and documentation for control system installations.
+ Assist in integrating control systems with data historians (e.g., PI) and MES.
+ Manage system backups and user accounts.
+ Contribute to Data Integrity and compliance programs.
**Project & Technical Support**
+ Collaborate with project teams and departments to develop and troubleshoot automation solutions.
+ Provide technical support for feasibility studies and field trials.
+ Support all stages of qualification (e.g., writing and executing test scripts, working with validation teams).
+ Participate in the rollout of new processes, including recipe development.
**Documentation & Training**
+ Develop and maintain SOPs for site control systems.
+ Create and deliver training for identified users to ensure proper system usage.
+ Cross-train team members to build department-wide automation knowledge.
+ Ensure proper documentation of activities, including SOP logs, EHS records, and logbooks.
**Compliance & Quality**
+ Ensure all activities comply with Takeda's quality standards, cGMP, EHS policies, and regulatory requirements.
+ Prepare reports related to deviations, investigations, and system changes.
+ Support internal audits and inspections where relevant.
**General Expectations**
+ Participate in ongoing training and development.
+ Uphold Takeda-ism values in daily work.
+ Foster a strong safety culture in collaboration with colleagues.
+ Respond to on-call or call-out situations as required.
+ Complete all required SOP readings, training, and assessments.
+ Perform other tasks as directed by the Director of Engineering or other designated leadership.
**What You Bring to Takeda**
+ Degree in Automation, Electrical, or related Engineering discipline.
+ 2-5 years of experience with automation/control systems.
+ Familiarity with Distributed Control Systems (DCS), especially Yokogawa Centum VP, is a plus.
+ Knowledge of Simatic S7 and TIA Portal is desirable.
+ Experience with Wonderware and PI Data Historian is advantageous.
+ Ability to develop IT/automation documentation and SOPs.
+ Strong project management and control system implementation skills.
**What you can look forward to with us:**
+ Competitive Salary: Including performance-based bonuses.
+ Retirement Plan: Employer contributions to your retirement plan.
+ Comprehensive Insurance: Employer-funded private medical insurance with dependants' cover, life insurance, and flexible options like dental insurance, partner life insurance, and serious illness protection.
+ Electric Charging Points: Available at parking locations.
+ Employee Assistance Program: Support for personal and professional challenges.
+ Wellbeing and Engagement: Dedicated teams to support your wellbeing.
+ Family-Friendly Policies: Supportive policies for a balanced work-life.
+ Generous Vacation: 26 vacation days plus additional days for service milestones and humanitarian volunteering leave.
+ Development Opportunities: Coaching, mentoring, educational programs, and formal training.
+ Subsidized Canteen: Enjoy meals at a reduced cost.
+ Flexible Benefits: Options like fuel card, bike to work, commuter ticket, and insurance deals.
**More about us:**
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
**Empowering our people to shine:**
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
If you are interested in this opportunity, we look forward to receiving your application via our online tool!
**Locations**
Grange Castle, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Fixed Term (Fixed Term)
**Time Type**
Full time
This advertiser has chosen not to accept applicants from your region.
1
DCS Automation Engineer ( FTC 30.04.2027)
Dublin, Leinster
Takeda Pharmaceuticals
Posted 2 days ago
Job Viewed
Job Description
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
**Automation Engineer**
This position is a **fixed-term role until 30 April 2027** .
At Takeda Grange Castle, our Automation Engineers play a vital role in operating and improving complex manufacturing systems while also supporting and training personnel. Responsibilities vary depending on the assignment, but the Automation Engineer will primarily work with multiple automation systems (PLC/SCADA/DCS) and supporting infrastructure.
This position requires both independent initiative and effective teamwork. The Automation Engineer supports daily operations, contributes to manufacturing goals, and ensures all work meets quality, safety, and environmental standards.
**Key Responsibilities :**
**Daily Operations & System Support**
+ Provide hands-on support for site activities related to PLC/SCADA/DCS systems.
+ Troubleshoot and resolve automation issues in collaboration with Manufacturing, Engineering, and EHS teams.
+ Implement code modifications as needed.
+ Provide accurate updates on task and project progress.
+ Support testing, debugging, and documentation for control system installations.
+ Assist in integrating control systems with data historians (e.g., PI) and MES.
+ Manage system backups and user accounts.
+ Contribute to Data Integrity and compliance programs.
**Project & Technical Support**
+ Collaborate with project teams and departments to develop and troubleshoot automation solutions.
+ Provide technical support for feasibility studies and field trials.
+ Support all stages of qualification (e.g., writing and executing test scripts, working with validation teams).
+ Participate in the rollout of new processes, including recipe development.
**Documentation & Training**
+ Develop and maintain SOPs for site control systems.
+ Create and deliver training for identified users to ensure proper system usage.
+ Cross-train team members to build department-wide automation knowledge.
+ Ensure proper documentation of activities, including SOP logs, EHS records, and logbooks.
**Compliance & Quality**
+ Ensure all activities comply with Takeda's quality standards, cGMP, EHS policies, and regulatory requirements.
+ Prepare reports related to deviations, investigations, and system changes.
+ Support internal audits and inspections where relevant.
**General Expectations**
+ Participate in ongoing training and development.
+ Uphold Takeda-ism values in daily work.
+ Foster a strong safety culture in collaboration with colleagues.
+ Respond to on-call or call-out situations as required.
+ Complete all required SOP readings, training, and assessments.
+ Perform other tasks as directed by the Director of Engineering or other designated leadership.
**What You Bring to Takeda**
+ Degree in Automation, Electrical, or related Engineering discipline.
+ 2-5 years of experience with automation/control systems.
+ Familiarity with Distributed Control Systems (DCS), especially Yokogawa Centum VP, is a plus.
+ Knowledge of Simatic S7 and TIA Portal is desirable.
+ Experience with Wonderware and PI Data Historian is advantageous.
+ Ability to develop IT/automation documentation and SOPs.
+ Strong project management and control system implementation skills.
**What you can look forward to with us:**
+ Competitive Salary: Including performance-based bonuses.
+ Retirement Plan: Employer contributions to your retirement plan.
+ Comprehensive Insurance: Employer-funded private medical insurance with dependants' cover, life insurance, and flexible options like dental insurance, partner life insurance, and serious illness protection.
+ Electric Charging Points: Available at parking locations.
+ Employee Assistance Program: Support for personal and professional challenges.
+ Wellbeing and Engagement: Dedicated teams to support your wellbeing.
+ Family-Friendly Policies: Supportive policies for a balanced work-life.
+ Generous Vacation: 26 vacation days plus additional days for service milestones and humanitarian volunteering leave.
+ Development Opportunities: Coaching, mentoring, educational programs, and formal training.
+ Subsidized Canteen: Enjoy meals at a reduced cost.
+ Flexible Benefits: Options like fuel card, bike to work, commuter ticket, and insurance deals.
**More about us:**
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
**Empowering our people to shine:**
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
If you are interested in this opportunity, we look forward to receiving your application via our online tool!
**Locations**
Grange Castle, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Fixed Term (Fixed Term)
**Time Type**
Full time
**Job Description**
**Automation Engineer**
This position is a **fixed-term role until 30 April 2027** .
At Takeda Grange Castle, our Automation Engineers play a vital role in operating and improving complex manufacturing systems while also supporting and training personnel. Responsibilities vary depending on the assignment, but the Automation Engineer will primarily work with multiple automation systems (PLC/SCADA/DCS) and supporting infrastructure.
This position requires both independent initiative and effective teamwork. The Automation Engineer supports daily operations, contributes to manufacturing goals, and ensures all work meets quality, safety, and environmental standards.
**Key Responsibilities :**
**Daily Operations & System Support**
+ Provide hands-on support for site activities related to PLC/SCADA/DCS systems.
+ Troubleshoot and resolve automation issues in collaboration with Manufacturing, Engineering, and EHS teams.
+ Implement code modifications as needed.
+ Provide accurate updates on task and project progress.
+ Support testing, debugging, and documentation for control system installations.
+ Assist in integrating control systems with data historians (e.g., PI) and MES.
+ Manage system backups and user accounts.
+ Contribute to Data Integrity and compliance programs.
**Project & Technical Support**
+ Collaborate with project teams and departments to develop and troubleshoot automation solutions.
+ Provide technical support for feasibility studies and field trials.
+ Support all stages of qualification (e.g., writing and executing test scripts, working with validation teams).
+ Participate in the rollout of new processes, including recipe development.
**Documentation & Training**
+ Develop and maintain SOPs for site control systems.
+ Create and deliver training for identified users to ensure proper system usage.
+ Cross-train team members to build department-wide automation knowledge.
+ Ensure proper documentation of activities, including SOP logs, EHS records, and logbooks.
**Compliance & Quality**
+ Ensure all activities comply with Takeda's quality standards, cGMP, EHS policies, and regulatory requirements.
+ Prepare reports related to deviations, investigations, and system changes.
+ Support internal audits and inspections where relevant.
**General Expectations**
+ Participate in ongoing training and development.
+ Uphold Takeda-ism values in daily work.
+ Foster a strong safety culture in collaboration with colleagues.
+ Respond to on-call or call-out situations as required.
+ Complete all required SOP readings, training, and assessments.
+ Perform other tasks as directed by the Director of Engineering or other designated leadership.
**What You Bring to Takeda**
+ Degree in Automation, Electrical, or related Engineering discipline.
+ 2-5 years of experience with automation/control systems.
+ Familiarity with Distributed Control Systems (DCS), especially Yokogawa Centum VP, is a plus.
+ Knowledge of Simatic S7 and TIA Portal is desirable.
+ Experience with Wonderware and PI Data Historian is advantageous.
+ Ability to develop IT/automation documentation and SOPs.
+ Strong project management and control system implementation skills.
**What you can look forward to with us:**
+ Competitive Salary: Including performance-based bonuses.
+ Retirement Plan: Employer contributions to your retirement plan.
+ Comprehensive Insurance: Employer-funded private medical insurance with dependants' cover, life insurance, and flexible options like dental insurance, partner life insurance, and serious illness protection.
+ Electric Charging Points: Available at parking locations.
+ Employee Assistance Program: Support for personal and professional challenges.
+ Wellbeing and Engagement: Dedicated teams to support your wellbeing.
+ Family-Friendly Policies: Supportive policies for a balanced work-life.
+ Generous Vacation: 26 vacation days plus additional days for service milestones and humanitarian volunteering leave.
+ Development Opportunities: Coaching, mentoring, educational programs, and formal training.
+ Subsidized Canteen: Enjoy meals at a reduced cost.
+ Flexible Benefits: Options like fuel card, bike to work, commuter ticket, and insurance deals.
**More about us:**
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
**Empowering our people to shine:**
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
If you are interested in this opportunity, we look forward to receiving your application via our online tool!
**Locations**
Grange Castle, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Fixed Term (Fixed Term)
**Time Type**
Full time
This advertiser has chosen not to accept applicants from your region.
2
Automation Engineer
Wicklow, Leinster
Takeda Pharmaceuticals
Posted 2 days ago
Job Viewed
Job Description
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
**People First** - At Takeda we are dedicated to improving the health and well-being of all people and bringing them the hope of a brighter future. It is our passion that transforms every job into meaningful action. Our people are the heart of Takeda.
For Takeda Ireland Ltd, we are looking for a
**Automation Engineer**
for a full-time permanent position at our location in Bray, Co. Wicklow, Ireland.
Are you passionate about cutting-edge technology and innovation? Join our team as an Automation Engineer, where you will be a Subject Matter Expert (SME) in Manufacturing Control Systems, Operational Technology, Machine Automation, and Digitalization. You will play a crucial role in ensuring the optimal performance of our automation systems and driving digital transformation projects.
**Your tasks in detail:**
+ Oversee automation systems to ensure maximum uptime and performance.
+ Manage system user access, backups, and restores.
+ Implement corrective actions and collaborate with vendor technical support.
+ Identify and execute small projects to enhance system performance.
+ Contribute to capital planning, project execution, and documentation.
+ Ensure all activities comply with site and corporate Quality Systems.
+ Create and maintain engineering deliverables and test scripts.
+ Develop and implement global automation strategies to standardize processes.
+ Maintain and optimize automation systems and infrastructure.
+ Develop solutions tailored to the manufacturing environment.
+ Drive automation projects, ensuring cost, schedule, and technical goals are met.
+ Stay updated with technology trends and benchmarks to keep Takeda at the forefront.
**Your profile:**
+ Degree in engineering (automation, robotics, computer science, etc.) or equivalent.
+ Minimum 5 years of work experience in GMP manufacturing, with expertise in automation. A broad understanding of pharmaceutical manufacturing processes and regulatory environments is essential. Experience in the pharmaceutical industry is advantageous.
+ Proficiency in automation solutions (Siemens, Omron, Mitsubishi, etc.). Knowledge of industry standards (GAMP, ANSI/ISA, 21 CFR Part 11, Annex 11) and GxP/QA. Familiarity with ANSI/ISA-99,100 standards is a plus.
+ Strong problem-solving and analytical skills, with experience in data analysis.
+ Ability to work in a team-based culture, engaging with internal and external stakeholders. Collaborate with Global Automation to implement best practices.
+ Contribute to the innovation roadmap and strategic planning. Mentor and train team members to enhance site expertise.
+ High communication skills, an analytical mindset, and the ability to work under pressure.
+ Fluent in written and spoken English
**What you can look forward to with us:**
+ Competitive Salary: Including performance-based bonuses.
+ Retirement Plan: Employer contributions to your retirement plan.
+ Comprehensive Insurance: Employer-funded private medical insurance with dependants' cover, life insurance, and flexible options like dental insurance, partner life insurance, and serious illness protection.
+ Electric Charging Points: Available at parking locations.
+ Employee Assistance Program: Support for personal and professional challenges.
+ Wellbeing and Engagement: Dedicated teams to support your wellbeing.
+ Family-Friendly Policies: Supportive policies for a balanced work-life.
+ Generous Vacation: 26 vacation days plus additional days for service milestones and humanitarian volunteering leave.
+ Development Opportunities: Coaching, mentoring, educational programs, and formal training.
+ Subsidized Canteen: Enjoy meals at a reduced cost.
+ Flexible Benefits: Options like fuel card, bike to work, commuter ticket, and insurance deals.
**More about us:**
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
**Empowering our people to shine:**
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
If you are interested in this opportunity, we look forward to receiving your application via our online tool!
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Regular
**Time Type**
Full time
**Job Description**
**People First** - At Takeda we are dedicated to improving the health and well-being of all people and bringing them the hope of a brighter future. It is our passion that transforms every job into meaningful action. Our people are the heart of Takeda.
For Takeda Ireland Ltd, we are looking for a
**Automation Engineer**
for a full-time permanent position at our location in Bray, Co. Wicklow, Ireland.
Are you passionate about cutting-edge technology and innovation? Join our team as an Automation Engineer, where you will be a Subject Matter Expert (SME) in Manufacturing Control Systems, Operational Technology, Machine Automation, and Digitalization. You will play a crucial role in ensuring the optimal performance of our automation systems and driving digital transformation projects.
**Your tasks in detail:**
+ Oversee automation systems to ensure maximum uptime and performance.
+ Manage system user access, backups, and restores.
+ Implement corrective actions and collaborate with vendor technical support.
+ Identify and execute small projects to enhance system performance.
+ Contribute to capital planning, project execution, and documentation.
+ Ensure all activities comply with site and corporate Quality Systems.
+ Create and maintain engineering deliverables and test scripts.
+ Develop and implement global automation strategies to standardize processes.
+ Maintain and optimize automation systems and infrastructure.
+ Develop solutions tailored to the manufacturing environment.
+ Drive automation projects, ensuring cost, schedule, and technical goals are met.
+ Stay updated with technology trends and benchmarks to keep Takeda at the forefront.
**Your profile:**
+ Degree in engineering (automation, robotics, computer science, etc.) or equivalent.
+ Minimum 5 years of work experience in GMP manufacturing, with expertise in automation. A broad understanding of pharmaceutical manufacturing processes and regulatory environments is essential. Experience in the pharmaceutical industry is advantageous.
+ Proficiency in automation solutions (Siemens, Omron, Mitsubishi, etc.). Knowledge of industry standards (GAMP, ANSI/ISA, 21 CFR Part 11, Annex 11) and GxP/QA. Familiarity with ANSI/ISA-99,100 standards is a plus.
+ Strong problem-solving and analytical skills, with experience in data analysis.
+ Ability to work in a team-based culture, engaging with internal and external stakeholders. Collaborate with Global Automation to implement best practices.
+ Contribute to the innovation roadmap and strategic planning. Mentor and train team members to enhance site expertise.
+ High communication skills, an analytical mindset, and the ability to work under pressure.
+ Fluent in written and spoken English
**What you can look forward to with us:**
+ Competitive Salary: Including performance-based bonuses.
+ Retirement Plan: Employer contributions to your retirement plan.
+ Comprehensive Insurance: Employer-funded private medical insurance with dependants' cover, life insurance, and flexible options like dental insurance, partner life insurance, and serious illness protection.
+ Electric Charging Points: Available at parking locations.
+ Employee Assistance Program: Support for personal and professional challenges.
+ Wellbeing and Engagement: Dedicated teams to support your wellbeing.
+ Family-Friendly Policies: Supportive policies for a balanced work-life.
+ Generous Vacation: 26 vacation days plus additional days for service milestones and humanitarian volunteering leave.
+ Development Opportunities: Coaching, mentoring, educational programs, and formal training.
+ Subsidized Canteen: Enjoy meals at a reduced cost.
+ Flexible Benefits: Options like fuel card, bike to work, commuter ticket, and insurance deals.
**More about us:**
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
**Empowering our people to shine:**
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
If you are interested in this opportunity, we look forward to receiving your application via our online tool!
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Regular
**Time Type**
Full time
This advertiser has chosen not to accept applicants from your region.
3
Quality & Reliability Engineer
Galway, Connacht
TE Connectivity
Posted 2 days ago
Job Viewed
Job Description
Quality & Reliability Engineer
**At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.**
**Job Overview**
Reporting to the Quality Manager/Quality Supervisor, the Quality Engineer is a member of the Quality group. The successful candidate will be responsible for Quality within their prescribed area of functional responsibility. They will be working as part of a team to maintain high quality/performance standards on all TE Connectivity products.
This challenging position will require an ability to work within a collaborative environment, pursuing continuous improvement and ensuring compliance to the TE Connectivity Quality System. The focus of the role is to supply high-quality medical devices and components to deliver an Extraordinary Customer Experience.
**Job Requirements**
+ Working cross functionally with other departments promote the achievement of the health and safety goals.
+ To deliver on all KPIs that help the business achieve its goal.
+ The Quality Engineer will perform an active role in further development and continuous improvement of the Quality Management system.
+ Establish and maintain risk management principles and methods throughout the product realization process in compliance with the company's Quality Management system and applicable regulations.
+ Maintain relevant documentation to comply with quality standards and customer requirements.
+ Offer quality guidance to the entire team in support of the day-to-day deliverables.
+ Develop strong links with customer organizations and other project stakeholders.
+ Support and initiate projects to ensure continuous improvement.
+ Quality review of responsible area validation documentation.
+ Investigation of root cause and implementation of effective corrective actions to prevent re-occurrence of compliance issues.
+ Overall responsibility for production GMP standards and compliance.Establish inspection standards, sampling plans and test methods where applicable.
+ Prepare and update procedures and associated documentation.
+ Support customer audits and surveillance/accreditation audits
+ Conduct and drive audits ensuring compliance with ISO13485.
+ The Quality Engineer will perform an active role in quality planning and new product introduction from a quality perspective.
+ Develop strong links with customer organizations and other project stakeholders.
+ Quality review of responsible area validation documentation
**What your background should look like**
**Qualifications**
+ Level 8 degree in Quality or Degree in Science / Engineering / Quality field.
+ Minimum of 2 years of industry experience is required.
**Key Requirements**
+ Working knowledge of FDA/ISO/MDD Quality systems for Medical Device companies.
+ Experience within a similar role as Quality Engineer is an advantage.
+ Quality experience in component and device manufacturing desirable.
+ Excellent written and oral communication skills essential.
**#jobsEMEANR**
**#LI-ONSITE**
**Competencies**
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork
**ABOUT TE CONNECTIVITY**
TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 9,000 engineers, working alongside customers in approximately 130 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at and on LinkedIn ( ,Facebook ( ,WeChat, ( Instagram andX (formerly Twitter). ( TE CONNECTIVITY OFFERS:**
We are pleased to offer you an exciting total package that can also be flexibly adapted to changing life situations - the well-being of our employees is our top priority!
- Competitive Salary Package
- Performance-Based Bonus Plans
- Health and Wellness Incentives
- Employee Stock Purchase Program
- Community Outreach Programs / Charity Events
- Employee Resource Group
**IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD**
TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from** **actual** **email addresses ending in @te.com** . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities.
Across our global sites and business units, we put together packages of benefits that are either supported by TE itself or provided by external service providers. In principle, the benefits offered can vary from site to site.
Location:
GALWAY, G, IE, H91 VN2T
City: GALWAY
State: G
Country/Region: IE
Travel: Less than 10%
Requisition ID:
Alternative Locations:
Function: Engineering & Technology
TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.
**At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.**
**Job Overview**
Reporting to the Quality Manager/Quality Supervisor, the Quality Engineer is a member of the Quality group. The successful candidate will be responsible for Quality within their prescribed area of functional responsibility. They will be working as part of a team to maintain high quality/performance standards on all TE Connectivity products.
This challenging position will require an ability to work within a collaborative environment, pursuing continuous improvement and ensuring compliance to the TE Connectivity Quality System. The focus of the role is to supply high-quality medical devices and components to deliver an Extraordinary Customer Experience.
**Job Requirements**
+ Working cross functionally with other departments promote the achievement of the health and safety goals.
+ To deliver on all KPIs that help the business achieve its goal.
+ The Quality Engineer will perform an active role in further development and continuous improvement of the Quality Management system.
+ Establish and maintain risk management principles and methods throughout the product realization process in compliance with the company's Quality Management system and applicable regulations.
+ Maintain relevant documentation to comply with quality standards and customer requirements.
+ Offer quality guidance to the entire team in support of the day-to-day deliverables.
+ Develop strong links with customer organizations and other project stakeholders.
+ Support and initiate projects to ensure continuous improvement.
+ Quality review of responsible area validation documentation.
+ Investigation of root cause and implementation of effective corrective actions to prevent re-occurrence of compliance issues.
+ Overall responsibility for production GMP standards and compliance.Establish inspection standards, sampling plans and test methods where applicable.
+ Prepare and update procedures and associated documentation.
+ Support customer audits and surveillance/accreditation audits
+ Conduct and drive audits ensuring compliance with ISO13485.
+ The Quality Engineer will perform an active role in quality planning and new product introduction from a quality perspective.
+ Develop strong links with customer organizations and other project stakeholders.
+ Quality review of responsible area validation documentation
**What your background should look like**
**Qualifications**
+ Level 8 degree in Quality or Degree in Science / Engineering / Quality field.
+ Minimum of 2 years of industry experience is required.
**Key Requirements**
+ Working knowledge of FDA/ISO/MDD Quality systems for Medical Device companies.
+ Experience within a similar role as Quality Engineer is an advantage.
+ Quality experience in component and device manufacturing desirable.
+ Excellent written and oral communication skills essential.
**#jobsEMEANR**
**#LI-ONSITE**
**Competencies**
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork
**ABOUT TE CONNECTIVITY**
TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 9,000 engineers, working alongside customers in approximately 130 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at and on LinkedIn ( ,Facebook ( ,WeChat, ( Instagram andX (formerly Twitter). ( TE CONNECTIVITY OFFERS:**
We are pleased to offer you an exciting total package that can also be flexibly adapted to changing life situations - the well-being of our employees is our top priority!
- Competitive Salary Package
- Performance-Based Bonus Plans
- Health and Wellness Incentives
- Employee Stock Purchase Program
- Community Outreach Programs / Charity Events
- Employee Resource Group
**IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD**
TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from** **actual** **email addresses ending in @te.com** . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities.
Across our global sites and business units, we put together packages of benefits that are either supported by TE itself or provided by external service providers. In principle, the benefits offered can vary from site to site.
Location:
GALWAY, G, IE, H91 VN2T
City: GALWAY
State: G
Country/Region: IE
Travel: Less than 10%
Requisition ID:
Alternative Locations:
Function: Engineering & Technology
TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.
This advertiser has chosen not to accept applicants from your region.
4
NPD Manufacturing & Process Dvl Engineer
Galway, Connacht
TE Connectivity
Posted 2 days ago
Job Viewed
Job Description
NPD Manufacturing & Process Dvl Engineer
**At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.**
**Job Overview**
The NPD (New Process Development) Manufacturing Engineer will be responsible for leading project-related Engineering activities within NPD and providing Engineering support to the Manufacturing department during the new product introduction cycle. In addition to this, the NPD Manufacturing Engineer will be responsible for the development of both existing and new process technologies as required by new products and prototypes.
**Job Requirements**
+ Work as part of the NPD team to drive product and process improvements.
+ Manage new designs through product lifecycle into manufacturing.
+ Work closely with Subject Matter Experts in the business to ensure all new products fit within Creganna Medical's existing manufacturing capability.
+ Work closely with Lean and Operations teams to ensure that any new processes developed meet world-class manufacturing standards.
+ Display customer focus always and be accountable for quality and timeliness of own work.
+ Manage a variable workload across different projects to meet NPD requirements.
+ Design and introduce manufacturing processes for new products to meet the demands of productivity and quality.
+ Ensure that complete and effective validations are carried out on all processes before transferring to manufacture including IQ, OQ, PQ & PPQ.
+ Identify and put in place permanent and effective technical/system solutions to problems.
+ Maintain high quality/compliance standards in line with Medical Device manufacturing requirements within Creganna Medical.
+ Applying Lean principles to identify and develop improvements that increase key process metrics of yield, throughput and productivity.
+ Investigate new process technologies and evaluate potential competitive advantage and the cost-benefit of introduction.
+ Manage external relationships with technology providers/suppliers.
+ Ensure that all Health, Safety and Environmental requirements are fulfilled.
**What your background should look like**
**Qualifications**
+ Level 8 Engineering degree, or equivalent qualification.
+ 2+ years' experience in a similar role.
**Key Requirements**
+ Strong mechanical background with a good working knowledge of metals processing a distinct advantage. Previous experience with laser cutting, laser welding or machining processes a distinct advantage.
+ Ability to develop process settings/windows using scientific methodology.
+ Knowledge of Six-Sigma methodology, problem-solving tools and Lean Manufacturing principles.
+ A demonstrated ability to solve problems with innovative and cost-effective solutions.
+ CAD, Solid works, Creo and Minitab experience preferable.
+ Experience working in a high-volume production environment would be beneficial.
+ Computer literate and familiar with all Office software packages.
+ Motivated to work on own initiative and the ability to make and implement decisions.
+ Excellent communication, planning and organizational skills
**#jobsEMEANR**
**#LI-ONSITE**
**Competencies**
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork
**ABOUT TE CONNECTIVITY**
TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 9,000 engineers, working alongside customers in approximately 130 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at and on LinkedIn ( ,Facebook ( ,WeChat, ( Instagram andX (formerly Twitter). ( TE CONNECTIVITY OFFERS:**
We are pleased to offer you an exciting total package that can also be flexibly adapted to changing life situations - the well-being of our employees is our top priority!
- Competitive Salary Package
- Performance-Based Bonus Plans
- Health and Wellness Incentives
- Employee Stock Purchase Program
- Community Outreach Programs / Charity Events
- Employee Resource Group
**IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD**
TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from** **actual** **email addresses ending in @te.com** . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities.
Across our global sites and business units, we put together packages of benefits that are either supported by TE itself or provided by external service providers. In principle, the benefits offered can vary from site to site.
Location:
GALWAY, G, IE, H91 VN2T
City: GALWAY
State: G
Country/Region: IE
Travel: Less than 10%
Requisition ID:
Alternative Locations:
Function: Engineering & Technology
TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.
**At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.**
**Job Overview**
The NPD (New Process Development) Manufacturing Engineer will be responsible for leading project-related Engineering activities within NPD and providing Engineering support to the Manufacturing department during the new product introduction cycle. In addition to this, the NPD Manufacturing Engineer will be responsible for the development of both existing and new process technologies as required by new products and prototypes.
**Job Requirements**
+ Work as part of the NPD team to drive product and process improvements.
+ Manage new designs through product lifecycle into manufacturing.
+ Work closely with Subject Matter Experts in the business to ensure all new products fit within Creganna Medical's existing manufacturing capability.
+ Work closely with Lean and Operations teams to ensure that any new processes developed meet world-class manufacturing standards.
+ Display customer focus always and be accountable for quality and timeliness of own work.
+ Manage a variable workload across different projects to meet NPD requirements.
+ Design and introduce manufacturing processes for new products to meet the demands of productivity and quality.
+ Ensure that complete and effective validations are carried out on all processes before transferring to manufacture including IQ, OQ, PQ & PPQ.
+ Identify and put in place permanent and effective technical/system solutions to problems.
+ Maintain high quality/compliance standards in line with Medical Device manufacturing requirements within Creganna Medical.
+ Applying Lean principles to identify and develop improvements that increase key process metrics of yield, throughput and productivity.
+ Investigate new process technologies and evaluate potential competitive advantage and the cost-benefit of introduction.
+ Manage external relationships with technology providers/suppliers.
+ Ensure that all Health, Safety and Environmental requirements are fulfilled.
**What your background should look like**
**Qualifications**
+ Level 8 Engineering degree, or equivalent qualification.
+ 2+ years' experience in a similar role.
**Key Requirements**
+ Strong mechanical background with a good working knowledge of metals processing a distinct advantage. Previous experience with laser cutting, laser welding or machining processes a distinct advantage.
+ Ability to develop process settings/windows using scientific methodology.
+ Knowledge of Six-Sigma methodology, problem-solving tools and Lean Manufacturing principles.
+ A demonstrated ability to solve problems with innovative and cost-effective solutions.
+ CAD, Solid works, Creo and Minitab experience preferable.
+ Experience working in a high-volume production environment would be beneficial.
+ Computer literate and familiar with all Office software packages.
+ Motivated to work on own initiative and the ability to make and implement decisions.
+ Excellent communication, planning and organizational skills
**#jobsEMEANR**
**#LI-ONSITE**
**Competencies**
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork
**ABOUT TE CONNECTIVITY**
TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 9,000 engineers, working alongside customers in approximately 130 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at and on LinkedIn ( ,Facebook ( ,WeChat, ( Instagram andX (formerly Twitter). ( TE CONNECTIVITY OFFERS:**
We are pleased to offer you an exciting total package that can also be flexibly adapted to changing life situations - the well-being of our employees is our top priority!
- Competitive Salary Package
- Performance-Based Bonus Plans
- Health and Wellness Incentives
- Employee Stock Purchase Program
- Community Outreach Programs / Charity Events
- Employee Resource Group
**IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD**
TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from** **actual** **email addresses ending in @te.com** . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities.
Across our global sites and business units, we put together packages of benefits that are either supported by TE itself or provided by external service providers. In principle, the benefits offered can vary from site to site.
Location:
GALWAY, G, IE, H91 VN2T
City: GALWAY
State: G
Country/Region: IE
Travel: Less than 10%
Requisition ID:
Alternative Locations:
Function: Engineering & Technology
TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.
This advertiser has chosen not to accept applicants from your region.
5
Manager Manufacturing Engineering
Galway, Connacht
TE Connectivity
Posted 2 days ago
Job Viewed
Job Description
Manager Manufacturing Engineering
**At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.**
**Job Overview**
Working within the core Engineering group, and reporting to the Site Engineering Manager, the Engineering Manager will lead a team of Engineers and Technicians and be responsible for managing and supporting all engineering activity in areas of responsibility. As a key member of the core Operations Support team, and as needs arise, the successful candidate will be expected to input to the development of supports and systems outside of core engineering responsibilities and assist in development and implementation of systems for areas as diverse as training, planning, staff supervision, and business processes.
**Job Requirements**
+ Health & Safety: Drive a Health & Safety culture, striving for Zero accidents through focus on Health and Safety initiatives in line with the plan objectives.
+ People: Coaching/mentoring and development of the employees using development plans and performance management. Identification and development of talent for succession planning.
+ Quality: Instill a Quality Culture of Right First-Time principles, driving yield improvements, Complaint reductions and supporting the CAPA process.
+ Continuous Improvement: Drive a Continuous Improvement culture, that aggressively targets reduction in costs of Poor Quality, increased efficiency in line with the Site targets, using Lean and six-sigma tools.
+ Service: Drives a culture of Exceptional Customer Experience (ECE) for both the Internal and External customers, by ensuring that projects and commitments and continually being met or exceeded.
+ New Product Introduction: Oversee and manage New Part Introduction in conjunction with the Prototyping / NPD Group.
+ Strategy: Develop and Drive the Engineering strategy through People Development, New technologies, validation ensuring the site is best suited for growth into the future.
+ Management of engineering budget to include the assembly of yearly budgets, adhering to budgets, instigating cost improvement projects to reduce budget spend and management of the capital expenditure programmed for the Business Unit.
+ Leading the engineering team in process designs, development, continuous improvement and any engineering aspects of technology transfer projects from other business units/sites. Identify and put in place permanent and effective solutions to technical/system problems.
+ Champion compliance to TE Connectivity Medical, part of TE Connectivity systems and processes.
+ Manages external relationships with key technology providers.
**What your background should look like**
**Qualifications**
+ Level 8 Engineering degree, or equivalent.
+ 5-7 years' experience in a high-volume demanding production environment.
**Key Requirements**
+ Knowledge of Medical Device or similar quality and manufacturing systems would be very desirable.
+ A demonstrated ability to lead a focused production / technical problem-solving team.
+ Working knowledge of six sigma and/or lean engineering principles with a proven track record in use and delivery of results.
+ Excellent communication skills, both oral and written along with an ability to communicate ideas, concepts, and projects clearly and positively.
+ Motivated to work on own initiative.
+ Ability to make and implement decisions.
#jobsEMEANR
#LI-ONSITE
**Competencies**
SET : Strategy, Execution, Talent (for managers)
**ABOUT TE CONNECTIVITY**
TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 9,000 engineers, working alongside customers in approximately 130 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at and on LinkedIn ( ,Facebook ( ,WeChat, ( Instagram andX (formerly Twitter). ( TE CONNECTIVITY OFFERS:**
We are pleased to offer you an exciting total package that can also be flexibly adapted to changing life situations - the well-being of our employees is our top priority!
- Competitive Salary Package
- Performance-Based Bonus Plans
- Health and Wellness Incentives
- Employee Stock Purchase Program
- Community Outreach Programs / Charity Events
- Employee Resource Group
**IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD**
TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from** **actual** **email addresses ending in @te.com** . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities.
Across our global sites and business units, we put together packages of benefits that are either supported by TE itself or provided by external service providers. In principle, the benefits offered can vary from site to site.
Location:
GALWAY, G, IE, H91 VN2T
City: GALWAY
State: G
Country/Region: IE
Travel: Less than 10%
Requisition ID:
Alternative Locations:
Function: Engineering & Technology
TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.
**At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.**
**Job Overview**
Working within the core Engineering group, and reporting to the Site Engineering Manager, the Engineering Manager will lead a team of Engineers and Technicians and be responsible for managing and supporting all engineering activity in areas of responsibility. As a key member of the core Operations Support team, and as needs arise, the successful candidate will be expected to input to the development of supports and systems outside of core engineering responsibilities and assist in development and implementation of systems for areas as diverse as training, planning, staff supervision, and business processes.
**Job Requirements**
+ Health & Safety: Drive a Health & Safety culture, striving for Zero accidents through focus on Health and Safety initiatives in line with the plan objectives.
+ People: Coaching/mentoring and development of the employees using development plans and performance management. Identification and development of talent for succession planning.
+ Quality: Instill a Quality Culture of Right First-Time principles, driving yield improvements, Complaint reductions and supporting the CAPA process.
+ Continuous Improvement: Drive a Continuous Improvement culture, that aggressively targets reduction in costs of Poor Quality, increased efficiency in line with the Site targets, using Lean and six-sigma tools.
+ Service: Drives a culture of Exceptional Customer Experience (ECE) for both the Internal and External customers, by ensuring that projects and commitments and continually being met or exceeded.
+ New Product Introduction: Oversee and manage New Part Introduction in conjunction with the Prototyping / NPD Group.
+ Strategy: Develop and Drive the Engineering strategy through People Development, New technologies, validation ensuring the site is best suited for growth into the future.
+ Management of engineering budget to include the assembly of yearly budgets, adhering to budgets, instigating cost improvement projects to reduce budget spend and management of the capital expenditure programmed for the Business Unit.
+ Leading the engineering team in process designs, development, continuous improvement and any engineering aspects of technology transfer projects from other business units/sites. Identify and put in place permanent and effective solutions to technical/system problems.
+ Champion compliance to TE Connectivity Medical, part of TE Connectivity systems and processes.
+ Manages external relationships with key technology providers.
**What your background should look like**
**Qualifications**
+ Level 8 Engineering degree, or equivalent.
+ 5-7 years' experience in a high-volume demanding production environment.
**Key Requirements**
+ Knowledge of Medical Device or similar quality and manufacturing systems would be very desirable.
+ A demonstrated ability to lead a focused production / technical problem-solving team.
+ Working knowledge of six sigma and/or lean engineering principles with a proven track record in use and delivery of results.
+ Excellent communication skills, both oral and written along with an ability to communicate ideas, concepts, and projects clearly and positively.
+ Motivated to work on own initiative.
+ Ability to make and implement decisions.
#jobsEMEANR
#LI-ONSITE
**Competencies**
SET : Strategy, Execution, Talent (for managers)
**ABOUT TE CONNECTIVITY**
TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 9,000 engineers, working alongside customers in approximately 130 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at and on LinkedIn ( ,Facebook ( ,WeChat, ( Instagram andX (formerly Twitter). ( TE CONNECTIVITY OFFERS:**
We are pleased to offer you an exciting total package that can also be flexibly adapted to changing life situations - the well-being of our employees is our top priority!
- Competitive Salary Package
- Performance-Based Bonus Plans
- Health and Wellness Incentives
- Employee Stock Purchase Program
- Community Outreach Programs / Charity Events
- Employee Resource Group
**IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD**
TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from** **actual** **email addresses ending in @te.com** . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities.
Across our global sites and business units, we put together packages of benefits that are either supported by TE itself or provided by external service providers. In principle, the benefits offered can vary from site to site.
Location:
GALWAY, G, IE, H91 VN2T
City: GALWAY
State: G
Country/Region: IE
Travel: Less than 10%
Requisition ID:
Alternative Locations:
Function: Engineering & Technology
TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.
This advertiser has chosen not to accept applicants from your region.
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6
Quality Assurance Specialist 3rd Party Products
Blanchardstown, Leinster
PCI Pharma Services
Posted 2 days ago
Job Viewed
Job Description
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Summary of Role
This is an exciting role as part of the Batch File Review Team. This role will appeal to anyone who enjoys a high degree of variety in their role. This role involves networking and communication across multiple stakeholders both internal and external to PCI. Batch file review encompasses all process types, OSD, Sterile, Biologics, Cell Therapy, Gene Therapy etc. Ideal grounding for anyone thinking of a future career as a QP.
· Part of the Batch File Review Team who:
a. Compile batch documents
b. Review batch documents in advance of QP review
c. Work with responsible site to complete corrections
d. Prepare COC for QP
e. Work closely with QP as issues arise and find resolution
· Perform a batch file review for batches manufactured/packed at PCI or in third party company.
· Raise Deviations, Corrective Action Requests, and Non-Conformance reports as required and in a timely manner and ensure that issues are communicated to the QA Manager/QP.
· Request Certificates of Analysis / Conformance for API/Drug Substance, Bulk Product, Packaging records from customers/suppliers. Review records against approved filing/Dossier of same.
· Coordination of every product supply chain flow - products which are coming from rest of the world and releasing to the European Union
· Participating customer meetings - discussion/collection/summary about the necessary quality documentation
· Writing SOPs or Work Instructions
· Maintenance of batch documents and retain samples in archive room. Update the PQR database after QP release.
· Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS Department.
· Carry out various other additional tasks that may be required from time to time in accordance with the overall goal of the company.
Knowledge / Skills & Experience
Essential:
· Degree and/or relevant experience.
· GMP experience
· Good communication skills.
· Steriles experience is desirable.
· Ability to problem solve.
· Capability to set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
· Minimum 2 yrs years' experience working in Quality Assurance
· Proven track record of showing how results were delivered through management/leadership of others.
· Capability to set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( Employment Opportunity (EEO) Statement:**
_PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._
_At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Summary of Role
This is an exciting role as part of the Batch File Review Team. This role will appeal to anyone who enjoys a high degree of variety in their role. This role involves networking and communication across multiple stakeholders both internal and external to PCI. Batch file review encompasses all process types, OSD, Sterile, Biologics, Cell Therapy, Gene Therapy etc. Ideal grounding for anyone thinking of a future career as a QP.
· Part of the Batch File Review Team who:
a. Compile batch documents
b. Review batch documents in advance of QP review
c. Work with responsible site to complete corrections
d. Prepare COC for QP
e. Work closely with QP as issues arise and find resolution
· Perform a batch file review for batches manufactured/packed at PCI or in third party company.
· Raise Deviations, Corrective Action Requests, and Non-Conformance reports as required and in a timely manner and ensure that issues are communicated to the QA Manager/QP.
· Request Certificates of Analysis / Conformance for API/Drug Substance, Bulk Product, Packaging records from customers/suppliers. Review records against approved filing/Dossier of same.
· Coordination of every product supply chain flow - products which are coming from rest of the world and releasing to the European Union
· Participating customer meetings - discussion/collection/summary about the necessary quality documentation
· Writing SOPs or Work Instructions
· Maintenance of batch documents and retain samples in archive room. Update the PQR database after QP release.
· Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS Department.
· Carry out various other additional tasks that may be required from time to time in accordance with the overall goal of the company.
Knowledge / Skills & Experience
Essential:
· Degree and/or relevant experience.
· GMP experience
· Good communication skills.
· Steriles experience is desirable.
· Ability to problem solve.
· Capability to set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
· Minimum 2 yrs years' experience working in Quality Assurance
· Proven track record of showing how results were delivered through management/leadership of others.
· Capability to set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( Employment Opportunity (EEO) Statement:**
_PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._
_At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled
This advertiser has chosen not to accept applicants from your region.
7
Quality Assurance Specialist 3rd Party Products
Drogheda, Leinster
PCI Pharma Services
Posted 2 days ago
Job Viewed
Job Description
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Summary of Role
This is an exciting role as part of the Batch File Review Team. This role will appeal to anyone who enjoys a high degree of variety in their role. This role involves networking and communication across multiple stakeholders both internal and external to PCI. Batch file review encompasses all process types, OSD, Sterile, Biologics, Cell Therapy, Gene Therapy etc. Ideal grounding for anyone thinking of a future career as a QP.
· Part of the Batch File Review Team who:
a. Compile batch documents
b. Review batch documents in advance of QP review
c. Work with responsible site to complete corrections
d. Prepare COC for QP
e. Work closely with QP as issues arise and find resolution
· Perform a batch file review for batches manufactured/packed at PCI or in third party company.
· Raise Deviations, Corrective Action Requests, and Non-Conformance reports as required and in a timely manner and ensure that issues are communicated to the QA Manager/QP.
· Request Certificates of Analysis / Conformance for API/Drug Substance, Bulk Product, Packaging records from customers/suppliers. Review records against approved filing/Dossier of same.
· Coordination of every product supply chain flow - products which are coming from rest of the world and releasing to the European Union
· Participating customer meetings - discussion/collection/summary about the necessary quality documentation
· Writing SOPs or Work Instructions
· Maintenance of batch documents and retain samples in archive room. Update the PQR database after QP release.
· Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS Department.
· Carry out various other additional tasks that may be required from time to time in accordance with the overall goal of the company.
Knowledge / Skills & Experience
Essential:
· Degree and/or relevant experience.
· GMP experience
· Good communication skills.
· Steriles experience is desirable.
· Ability to problem solve.
· Capability to set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
· Minimum 2 yrs years' experience working in Quality Assurance
· Proven track record of showing how results were delivered through management/leadership of others.
· Capability to set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( Employment Opportunity (EEO) Statement:**
_PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._
_At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Summary of Role
This is an exciting role as part of the Batch File Review Team. This role will appeal to anyone who enjoys a high degree of variety in their role. This role involves networking and communication across multiple stakeholders both internal and external to PCI. Batch file review encompasses all process types, OSD, Sterile, Biologics, Cell Therapy, Gene Therapy etc. Ideal grounding for anyone thinking of a future career as a QP.
· Part of the Batch File Review Team who:
a. Compile batch documents
b. Review batch documents in advance of QP review
c. Work with responsible site to complete corrections
d. Prepare COC for QP
e. Work closely with QP as issues arise and find resolution
· Perform a batch file review for batches manufactured/packed at PCI or in third party company.
· Raise Deviations, Corrective Action Requests, and Non-Conformance reports as required and in a timely manner and ensure that issues are communicated to the QA Manager/QP.
· Request Certificates of Analysis / Conformance for API/Drug Substance, Bulk Product, Packaging records from customers/suppliers. Review records against approved filing/Dossier of same.
· Coordination of every product supply chain flow - products which are coming from rest of the world and releasing to the European Union
· Participating customer meetings - discussion/collection/summary about the necessary quality documentation
· Writing SOPs or Work Instructions
· Maintenance of batch documents and retain samples in archive room. Update the PQR database after QP release.
· Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS Department.
· Carry out various other additional tasks that may be required from time to time in accordance with the overall goal of the company.
Knowledge / Skills & Experience
Essential:
· Degree and/or relevant experience.
· GMP experience
· Good communication skills.
· Steriles experience is desirable.
· Ability to problem solve.
· Capability to set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
· Minimum 2 yrs years' experience working in Quality Assurance
· Proven track record of showing how results were delivered through management/leadership of others.
· Capability to set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( Employment Opportunity (EEO) Statement:**
_PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._
_At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled
This advertiser has chosen not to accept applicants from your region.
8
Quality Assurance Specialist 3rd Party Products
PCI Pharma Services
Posted 2 days ago
Job Viewed
Job Description
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Summary of Role
This is an exciting role as part of the Batch File Review Team. This role will appeal to anyone who enjoys a high degree of variety in their role. This role involves networking and communication across multiple stakeholders both internal and external to PCI. Batch file review encompasses all process types, OSD, Sterile, Biologics, Cell Therapy, Gene Therapy etc. Ideal grounding for anyone thinking of a future career as a QP.
· Part of the Batch File Review Team who:
a. Compile batch documents
b. Review batch documents in advance of QP review
c. Work with responsible site to complete corrections
d. Prepare COC for QP
e. Work closely with QP as issues arise and find resolution
· Perform a batch file review for batches manufactured/packed at PCI or in third party company.
· Raise Deviations, Corrective Action Requests, and Non-Conformance reports as required and in a timely manner and ensure that issues are communicated to the QA Manager/QP.
· Request Certificates of Analysis / Conformance for API/Drug Substance, Bulk Product, Packaging records from customers/suppliers. Review records against approved filing/Dossier of same.
· Coordination of every product supply chain flow - products which are coming from rest of the world and releasing to the European Union
· Participating customer meetings - discussion/collection/summary about the necessary quality documentation
· Writing SOPs or Work Instructions
· Maintenance of batch documents and retain samples in archive room. Update the PQR database after QP release.
· Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS Department.
· Carry out various other additional tasks that may be required from time to time in accordance with the overall goal of the company.
Knowledge / Skills & Experience
Essential:
· Degree and/or relevant experience.
· GMP experience
· Good communication skills.
· Steriles experience is desirable.
· Ability to problem solve.
· Capability to set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
· Minimum 2 yrs years' experience working in Quality Assurance
· Proven track record of showing how results were delivered through management/leadership of others.
· Capability to set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( Employment Opportunity (EEO) Statement:**
_PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._
_At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Summary of Role
This is an exciting role as part of the Batch File Review Team. This role will appeal to anyone who enjoys a high degree of variety in their role. This role involves networking and communication across multiple stakeholders both internal and external to PCI. Batch file review encompasses all process types, OSD, Sterile, Biologics, Cell Therapy, Gene Therapy etc. Ideal grounding for anyone thinking of a future career as a QP.
· Part of the Batch File Review Team who:
a. Compile batch documents
b. Review batch documents in advance of QP review
c. Work with responsible site to complete corrections
d. Prepare COC for QP
e. Work closely with QP as issues arise and find resolution
· Perform a batch file review for batches manufactured/packed at PCI or in third party company.
· Raise Deviations, Corrective Action Requests, and Non-Conformance reports as required and in a timely manner and ensure that issues are communicated to the QA Manager/QP.
· Request Certificates of Analysis / Conformance for API/Drug Substance, Bulk Product, Packaging records from customers/suppliers. Review records against approved filing/Dossier of same.
· Coordination of every product supply chain flow - products which are coming from rest of the world and releasing to the European Union
· Participating customer meetings - discussion/collection/summary about the necessary quality documentation
· Writing SOPs or Work Instructions
· Maintenance of batch documents and retain samples in archive room. Update the PQR database after QP release.
· Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS Department.
· Carry out various other additional tasks that may be required from time to time in accordance with the overall goal of the company.
Knowledge / Skills & Experience
Essential:
· Degree and/or relevant experience.
· GMP experience
· Good communication skills.
· Steriles experience is desirable.
· Ability to problem solve.
· Capability to set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
· Minimum 2 yrs years' experience working in Quality Assurance
· Proven track record of showing how results were delivered through management/leadership of others.
· Capability to set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( Employment Opportunity (EEO) Statement:**
_PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._
_At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled
This advertiser has chosen not to accept applicants from your region.
9