7 Manufacturing jobs in Westport
Senior Manufacturing Analyst
Westport, Connacht
AbbVie
Posted 2 days ago
Job Viewed
Job Description
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are looking for a Senior Manufacturing Analyst for our site in Westport, in our core 2 and core 3 parts of our facility, this will be a shift position rotation 24/7.
You will provide support to the Manufacturing Technicians and Manufacturing Analysts in achieving the overall business goals and objectives for the site.
As part of the role, you will be responsible for the day to day running of the shift - from the shift handover from the previous shift to the handover to the next shift by delegating the tasks accordingly.
As issues arise on shift they are to be communicated by the Manufacturing Technicians and Analysts to the Senior Manufacturing Analyst, who in turn escalates them to the Technical Shift Lead as required. They are then responsible for re-arranging and re-assigning shift schedule / tasks / indirect reports as issues arise.
Responsibilities:
- Ensure that all areas of responsibility are fully staffed and that any constraints are managed appropriately or escalated to the Manufacturing Manager.
- Ensure all activities are completed in line with regulatory (QA and EHS) and corporate requirements.
- Manage product improvement changes and implementation process improvements
- Lead and support Continuous Improvement initiatives as required to support the overall goals of the Manufacturing Department
- Develop, implement and maintain operational excellence methods of working within the manufacturing team in conjunction with the shift manager
- Ensure all activities of the Manufacturing Department are performed in accordance with compliance requirements, GMP, OPEX standards and relevant SOPs and policies through Process Confirmation where appropriate.
- Provide leadership at the tiered OPEX meetings to ensure focus and traction is maintained on the key objectives
- Co-ordination with maintenance department, validations and water engineers as issues arise to ensure that they are investigated and addressed in a timely manner
- Liaise with packaging and warehouse personnel in resolving SAP batch / component related issues in a timely manner
- Support and ensure QMS is maintained to a high standard
- Ensure shift updates and issues are communicated, highlight any issues with schedule adherence
- Ensure team members are cross trained, and training is progressed in a timely manner. Actively participate in the training and certification of new employees.
Qualifications
+ Bachelor's Degree in a pharmaceutical science/ engineering / operations discipline.
+ Minimum of 3 years relevant experience in Pharma/Medical Devices/Food Operations
+ Clear understanding of working within a regulated environment
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are looking for a Senior Manufacturing Analyst for our site in Westport, in our core 2 and core 3 parts of our facility, this will be a shift position rotation 24/7.
You will provide support to the Manufacturing Technicians and Manufacturing Analysts in achieving the overall business goals and objectives for the site.
As part of the role, you will be responsible for the day to day running of the shift - from the shift handover from the previous shift to the handover to the next shift by delegating the tasks accordingly.
As issues arise on shift they are to be communicated by the Manufacturing Technicians and Analysts to the Senior Manufacturing Analyst, who in turn escalates them to the Technical Shift Lead as required. They are then responsible for re-arranging and re-assigning shift schedule / tasks / indirect reports as issues arise.
Responsibilities:
- Ensure that all areas of responsibility are fully staffed and that any constraints are managed appropriately or escalated to the Manufacturing Manager.
- Ensure all activities are completed in line with regulatory (QA and EHS) and corporate requirements.
- Manage product improvement changes and implementation process improvements
- Lead and support Continuous Improvement initiatives as required to support the overall goals of the Manufacturing Department
- Develop, implement and maintain operational excellence methods of working within the manufacturing team in conjunction with the shift manager
- Ensure all activities of the Manufacturing Department are performed in accordance with compliance requirements, GMP, OPEX standards and relevant SOPs and policies through Process Confirmation where appropriate.
- Provide leadership at the tiered OPEX meetings to ensure focus and traction is maintained on the key objectives
- Co-ordination with maintenance department, validations and water engineers as issues arise to ensure that they are investigated and addressed in a timely manner
- Liaise with packaging and warehouse personnel in resolving SAP batch / component related issues in a timely manner
- Support and ensure QMS is maintained to a high standard
- Ensure shift updates and issues are communicated, highlight any issues with schedule adherence
- Ensure team members are cross trained, and training is progressed in a timely manner. Actively participate in the training and certification of new employees.
Qualifications
+ Bachelor's Degree in a pharmaceutical science/ engineering / operations discipline.
+ Minimum of 3 years relevant experience in Pharma/Medical Devices/Food Operations
+ Clear understanding of working within a regulated environment
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
This advertiser has chosen not to accept applicants from your region.
0
Senior Quality Analyst- Manufacturing
Shannon, Munster
Zimmer Biomet
Posted 2 days ago
Job Viewed
Job Description
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.
**What You Can Expect**
The purpose of this position is to provide direct user support for Manufacturing systems, such as MES and Delmia. Duties include updating of functional specifications, software, data, workflows and trouble shooting. The person will act as a cross-functional, inter-business unit resource which ensures our automated quality processes are compliant with all applicable regulations. As such, the incumbent must be technically knowledgeable in multiple disciplines including information technology, quality, and GxP processes.
**How You'll Create Impact**
+ Facilitates and / or provides support for all application users, including training and trouble shooting.
+ Act as technical expert for system requirements and updates.
+ Ensure systems are available, globally 7x24. Includes troubleshooting and problem resolution.
+ Support activities for process and system improvements, focusing on compliant, yet lean initiatives.
+ Manage and confront issues as they arise.
+ Formulate cross-functional teams, gaining consensus of requirements and approach and global teams
+ Prepares and assures completion of required personnel training.
+ Proactively works to ensure automated systems related to quality systems meet or exceed all applicable regulations and standards.
+ Lead procedures and validation activities for any manufacturing software system tools
**What Makes You Stand Out**
+ Ideally possesses a broad business perspective, including understanding the processes used within the respective areas, project management and Zimmer business goals of cost, quality and customer satisfaction
+ Must work well with others and interact effectively with all levels, technical information, outside contacts and support personnel.
+ Must be creative in solving problems with new products to maintain scheduled completion dates.
+ Must possess an understanding of GxP regulations, state of the art validation techniques.
+ Must be able to develop, implement, and execute system protocols.
+ Requires an understanding of process, equipment, software, and infrastructure, with an emphasis on software.
+ Requires knowledge of Systems.
**Your Background**
+ Bachelor's degree in computer science or an appropriate engineering discipline
+ A minimum of one year of experience supporting applications is required
+ Familiarity with Good Manufacturing Practices and QSR/ISO standards required.
+ 5-7 years plus professional work experience required.
EOE/M/F/Vet/Disability
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.
**What You Can Expect**
The purpose of this position is to provide direct user support for Manufacturing systems, such as MES and Delmia. Duties include updating of functional specifications, software, data, workflows and trouble shooting. The person will act as a cross-functional, inter-business unit resource which ensures our automated quality processes are compliant with all applicable regulations. As such, the incumbent must be technically knowledgeable in multiple disciplines including information technology, quality, and GxP processes.
**How You'll Create Impact**
+ Facilitates and / or provides support for all application users, including training and trouble shooting.
+ Act as technical expert for system requirements and updates.
+ Ensure systems are available, globally 7x24. Includes troubleshooting and problem resolution.
+ Support activities for process and system improvements, focusing on compliant, yet lean initiatives.
+ Manage and confront issues as they arise.
+ Formulate cross-functional teams, gaining consensus of requirements and approach and global teams
+ Prepares and assures completion of required personnel training.
+ Proactively works to ensure automated systems related to quality systems meet or exceed all applicable regulations and standards.
+ Lead procedures and validation activities for any manufacturing software system tools
**What Makes You Stand Out**
+ Ideally possesses a broad business perspective, including understanding the processes used within the respective areas, project management and Zimmer business goals of cost, quality and customer satisfaction
+ Must work well with others and interact effectively with all levels, technical information, outside contacts and support personnel.
+ Must be creative in solving problems with new products to maintain scheduled completion dates.
+ Must possess an understanding of GxP regulations, state of the art validation techniques.
+ Must be able to develop, implement, and execute system protocols.
+ Requires an understanding of process, equipment, software, and infrastructure, with an emphasis on software.
+ Requires knowledge of Systems.
**Your Background**
+ Bachelor's degree in computer science or an appropriate engineering discipline
+ A minimum of one year of experience supporting applications is required
+ Familiarity with Good Manufacturing Practices and QSR/ISO standards required.
+ 5-7 years plus professional work experience required.
EOE/M/F/Vet/Disability
This advertiser has chosen not to accept applicants from your region.
1
Manufacturing Specialist (Central Services)
Westport, Connacht
AbbVie
Posted 2 days ago
Job Viewed
Job Description
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
AbbVie helps people around the world live better days and better lives each year. And that takes all of us.
We are now recruiting for a Manufacturing Specialist to join our newly formed Central Cervices Team in AbbVie Westport, Co Mayo.
Established in 1977, AbbVie Westport is a Centre of Excellence for Aseptic for Commercial manufacturing of Biologics & Eyecare (pharmaceutical) products. In this role you will assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, achieve desired financial performance including cost reductions, and build an inclusive culture of high performance as part of the team. Your main focus will be working on process improvement projects with cross-functional teams.
This is a great opportunity to make a large impact of the future success of manufacturing eyecare products to our patients, working with a multitude of pharmaceutical manufacturing technologies, such as mold blowing, single dose, multidose and steroid manufacturing.
If you are looking for a career with impact, then come and join us in our mission to provide the highest quality products and outstanding service to our patients!
Is this a team you want to be part of? Then read on.
Key responsibilities:
+ Support the production schedule according to customer demands from a technical perspective where and when required.
+ Participate in performance management across the department and ensure consistency in approach from a technical perspective and aid in communication between different stakeholders. Track and measure departmental KPIs and translate them into Perfect Index relevant KPIs.
+ Lead and promote a culture of Safety, Quality, Excellence, Continuous Improvement and drive lean initiatives by regular production GEMBAs
+ Technical knowledge in the manufactured products and production equipment used.
+ Support lean manufacturing on site by writing/ updating and approving SOPs
+ Lead production related product quality investigations in conjunction with Quality Assurance and other cross-functional stakeholders including the assignment and management of corrective and preventive actions. Apply investigational tools like fishbone, 5W, contradiction matrix for root cause analysis.
+ Ensure compliance with applicable regulatory agencies by supporting where required, also use knowledge to drive continuity and improvement on an ongoing basis
+ Support change management and lead production aspect of CPs as part of a cross-functional team including identification and implementation of relevant tasks in a timely manner.
+ Conduct business in compliance with all applicable laws and regulations, company policies and with highest ethical standards.
+ Support operations in maintaining a high 5S standard
+ Ensure you are fully informed of Shift and Dept performance metrics and have a clear understanding on how they impact overall Site Perfect Index
Qualifications
So, what do you need to do this role?
Technical Skills and Experience:
+ BSc in Engineering, Science, a relevant discipline, or equivalent experience required, MSc in Engineering, Science, or a relevant discipline preferred
+ 2+ years in a GMP manufacturing environment (equivalent experience considered), aseptic manufacturing experience preferred
+ Excellent documentation and communication skills
+ Excellent analytical and presentation skills with the ability to work independently
+ Ability to work towards strict deadlines
+ Ability to build relationships with peers, influence without authority
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
AbbVie helps people around the world live better days and better lives each year. And that takes all of us.
We are now recruiting for a Manufacturing Specialist to join our newly formed Central Cervices Team in AbbVie Westport, Co Mayo.
Established in 1977, AbbVie Westport is a Centre of Excellence for Aseptic for Commercial manufacturing of Biologics & Eyecare (pharmaceutical) products. In this role you will assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, achieve desired financial performance including cost reductions, and build an inclusive culture of high performance as part of the team. Your main focus will be working on process improvement projects with cross-functional teams.
This is a great opportunity to make a large impact of the future success of manufacturing eyecare products to our patients, working with a multitude of pharmaceutical manufacturing technologies, such as mold blowing, single dose, multidose and steroid manufacturing.
If you are looking for a career with impact, then come and join us in our mission to provide the highest quality products and outstanding service to our patients!
Is this a team you want to be part of? Then read on.
Key responsibilities:
+ Support the production schedule according to customer demands from a technical perspective where and when required.
+ Participate in performance management across the department and ensure consistency in approach from a technical perspective and aid in communication between different stakeholders. Track and measure departmental KPIs and translate them into Perfect Index relevant KPIs.
+ Lead and promote a culture of Safety, Quality, Excellence, Continuous Improvement and drive lean initiatives by regular production GEMBAs
+ Technical knowledge in the manufactured products and production equipment used.
+ Support lean manufacturing on site by writing/ updating and approving SOPs
+ Lead production related product quality investigations in conjunction with Quality Assurance and other cross-functional stakeholders including the assignment and management of corrective and preventive actions. Apply investigational tools like fishbone, 5W, contradiction matrix for root cause analysis.
+ Ensure compliance with applicable regulatory agencies by supporting where required, also use knowledge to drive continuity and improvement on an ongoing basis
+ Support change management and lead production aspect of CPs as part of a cross-functional team including identification and implementation of relevant tasks in a timely manner.
+ Conduct business in compliance with all applicable laws and regulations, company policies and with highest ethical standards.
+ Support operations in maintaining a high 5S standard
+ Ensure you are fully informed of Shift and Dept performance metrics and have a clear understanding on how they impact overall Site Perfect Index
Qualifications
So, what do you need to do this role?
Technical Skills and Experience:
+ BSc in Engineering, Science, a relevant discipline, or equivalent experience required, MSc in Engineering, Science, or a relevant discipline preferred
+ 2+ years in a GMP manufacturing environment (equivalent experience considered), aseptic manufacturing experience preferred
+ Excellent documentation and communication skills
+ Excellent analytical and presentation skills with the ability to work independently
+ Ability to work towards strict deadlines
+ Ability to build relationships with peers, influence without authority
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
This advertiser has chosen not to accept applicants from your region.
2
Manufacturing Shift Manager - Biologics
Westport, Connacht
AbbVie
Posted 2 days ago
Job Viewed
Job Description
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X ( , Facebook, Instagram ( , YouTube and LinkedIn.
Job Description
Do your best work at AbbVie-as part of a brilliant, curious team
We are currently sourcing an experienced Manufacturing Shift Manager to join our Biologics Manufacturing team in AbbVie Westport on a permanent basis. In this role you will lead and facilitate the safe operations of the 24/7 Biologics manufacturing team in a bio-pharmaceutical processing facility in line with all safety, regulatory and operational requirements.
This is a shift based role, you will be required to work 12-hour shifts between days and nights on a monthly rotation.
As part of your new and exciting role you will assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, achieve desired financial performance including cost reductions, and build a culture of high performance for the team
Does this interest to you? then read on.
Here's a snapshot of your key responsibilities for this role:
+ Act as key point of technical contact for aseptic fill finish activities.
+ Supervision and execution of compounding, filling, lyophilization, equipment preparation, formulation, buffer preparation and support processing activities in the biologics fill finish facility to meet clearly stated operating objectives
+ You will lead, coach & mentor your manufacturing team, across a 12-hour rotating shift, to maximize the effectiveness through clear and effective communication of task details and goals to their team members, to allow the biologics technicians to work effectively
+ As part of this diverse and inclusive team, you will conduct on the floor promotion of a culture of contamination control and compliance with aseptic best practice.
+ Communicate the departmental goals, to provide cost effective quality compliant products in a safe, effective manner
+ We believe in collaboration so in this role, you will liaise with program management, supply chain, technical operations quality and engineering groups to ensure effective planning, scheduling and execution of commercial and NPI clinical manufacturing
+ Resolve operations/project issues by working with team members, project customers, and others as appropriate.
+ Responsible for driving operations excellences and Key operations targets including OEE where applicable
+ Provides direct interface as a subject matter expert with QA department to interaction with HPRA, FDA and applicable health authority and internal audits
Qualifications
So, what do you need to do this role?
+ Minimum of 3 year's experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry.
+ A minimum of 1 year team direct supervisory experience in a team environment
+ 3rd level qualification in a Science, Engineering or related scientific field, advanced degree is preferred
+ Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
+ Comprehensive understanding of the principles of contamination control and regulatory expectations for aseptic processing.
+ Has a technical background in pharmaceutical, biologics, or similar industries
+ Flexibility with working 12-hour shift, rotating between days and nights on a monthly rotation
+ Possess a strong technical knowledge and application of concepts, practices, and procedures. Works on problems of complex scope where analysis of situations or data involves multiple competing factors. Exercises judgment and advises management as to the appropriate actions
So, are you ready now lead this ambitious and diverse Manufacturing team? Apply today!
It's important to remember, AbbVie is an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment.
Additional Information
All your information will be kept confidential according to EEO guidelines.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X ( , Facebook, Instagram ( , YouTube and LinkedIn.
Job Description
Do your best work at AbbVie-as part of a brilliant, curious team
We are currently sourcing an experienced Manufacturing Shift Manager to join our Biologics Manufacturing team in AbbVie Westport on a permanent basis. In this role you will lead and facilitate the safe operations of the 24/7 Biologics manufacturing team in a bio-pharmaceutical processing facility in line with all safety, regulatory and operational requirements.
This is a shift based role, you will be required to work 12-hour shifts between days and nights on a monthly rotation.
As part of your new and exciting role you will assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, achieve desired financial performance including cost reductions, and build a culture of high performance for the team
Does this interest to you? then read on.
Here's a snapshot of your key responsibilities for this role:
+ Act as key point of technical contact for aseptic fill finish activities.
+ Supervision and execution of compounding, filling, lyophilization, equipment preparation, formulation, buffer preparation and support processing activities in the biologics fill finish facility to meet clearly stated operating objectives
+ You will lead, coach & mentor your manufacturing team, across a 12-hour rotating shift, to maximize the effectiveness through clear and effective communication of task details and goals to their team members, to allow the biologics technicians to work effectively
+ As part of this diverse and inclusive team, you will conduct on the floor promotion of a culture of contamination control and compliance with aseptic best practice.
+ Communicate the departmental goals, to provide cost effective quality compliant products in a safe, effective manner
+ We believe in collaboration so in this role, you will liaise with program management, supply chain, technical operations quality and engineering groups to ensure effective planning, scheduling and execution of commercial and NPI clinical manufacturing
+ Resolve operations/project issues by working with team members, project customers, and others as appropriate.
+ Responsible for driving operations excellences and Key operations targets including OEE where applicable
+ Provides direct interface as a subject matter expert with QA department to interaction with HPRA, FDA and applicable health authority and internal audits
Qualifications
So, what do you need to do this role?
+ Minimum of 3 year's experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry.
+ A minimum of 1 year team direct supervisory experience in a team environment
+ 3rd level qualification in a Science, Engineering or related scientific field, advanced degree is preferred
+ Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
+ Comprehensive understanding of the principles of contamination control and regulatory expectations for aseptic processing.
+ Has a technical background in pharmaceutical, biologics, or similar industries
+ Flexibility with working 12-hour shift, rotating between days and nights on a monthly rotation
+ Possess a strong technical knowledge and application of concepts, practices, and procedures. Works on problems of complex scope where analysis of situations or data involves multiple competing factors. Exercises judgment and advises management as to the appropriate actions
So, are you ready now lead this ambitious and diverse Manufacturing team? Apply today!
It's important to remember, AbbVie is an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment.
Additional Information
All your information will be kept confidential according to EEO guidelines.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
This advertiser has chosen not to accept applicants from your region.
3
Biologics (Manufacturing) Technical Shift Lead
Westport, Connacht
AbbVie
Posted 2 days ago
Job Viewed
Job Description
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X ( , Facebook, Instagram ( , YouTube and LinkedIn.
Job Description
Our pipeline holds the promise of medicines and solutions that could treat 1.6+ billion people. Learn more about bringing this promise to life.
Welcome to AbbVie!
AbbVie employees work every single day to discover and address many of the world's most pressing health challenges. Our work helps people live better lives. When you have patients depending on your solutions, you look for the best people, and when we find them, we make it our business to treat them well.
Our Westport team invites technical experts to join our NPI Biopharma operations team as our new Technical Shift Leader. In the role, you will have the opportunity to lead an established team developing and guiding its members technically and professionally.
This is a shift based role, you will be required to work 12-hour shifts between days and nights on a monthly rotation.
Delivering high levels of customer service, in this role, you will ensure the quality of the product, comply with all regulatory requirements, achieve desired financial performance, including cost reductions, and build a high-performance culture for the team.
If great benefits, a defined career path, and work-life balance are important in your next career move, then read on to find out more:
Key activities:
+ Act as your team's key point of contact and technical expert.
+ Lead and support your team to deliver compounding, filling, lyophilization, equipment preparation, formulation, buffer preparation and processing activities in the biologics fill-finish facility to meet clearly stated operating objectives
+ Coach & mentor your manufacturing team to maximize its effectiveness through clear and effective communication
+ Promote and develop a culture of contamination control and compliance with aseptic best practices
+ Communicate departmental goals to provide cost-effective quality compliant products in a safe, effective manner
+ Collaborate with program management, supply chain, technical operations, quality, and engineering groups to ensure effective planning, scheduling and execution of commercial and NPI clinical manufacturing
+ Resolve operations/project issues with team members, project customers, and others as appropriate.
+ Drive operations excellence and key operations targets, including OEE where applicable
+ Provide direct interface as a subject matter expert with the QA department to interact with HPRA, FDA and applicable health authorities and internal audits.
Qualifications
So what will you need to be successful in this role?
Education and preferred experience:
+ Minimum of 5 years experience in batch processing, automation, commissioning, and/or validation in an FDA/HHPRA-regulated industry.
+ Bachelor's degree in chemistry, pharmacy, engineering or a related scientific field is required; an advanced degree is preferred.
+ Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
+ Comprehensive understanding of contamination control principles and regulatory expectations for aseptic processing.
+ Technical background in pharmaceutical, biologics, or similar industries.
+ A minimum of 1 year of direct supervisory experience in a team environment is preferred
+ Possess strong technical knowledge and application of concepts, practices, and procedures. Works on problems of complex scope where analysis of situations or data involves multiple competing factors. Exercises judgment and advises the appropriate actions
Additional Information
All your information will be kept confidential according to EEO guidelines.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X ( , Facebook, Instagram ( , YouTube and LinkedIn.
Job Description
Our pipeline holds the promise of medicines and solutions that could treat 1.6+ billion people. Learn more about bringing this promise to life.
Welcome to AbbVie!
AbbVie employees work every single day to discover and address many of the world's most pressing health challenges. Our work helps people live better lives. When you have patients depending on your solutions, you look for the best people, and when we find them, we make it our business to treat them well.
Our Westport team invites technical experts to join our NPI Biopharma operations team as our new Technical Shift Leader. In the role, you will have the opportunity to lead an established team developing and guiding its members technically and professionally.
This is a shift based role, you will be required to work 12-hour shifts between days and nights on a monthly rotation.
Delivering high levels of customer service, in this role, you will ensure the quality of the product, comply with all regulatory requirements, achieve desired financial performance, including cost reductions, and build a high-performance culture for the team.
If great benefits, a defined career path, and work-life balance are important in your next career move, then read on to find out more:
Key activities:
+ Act as your team's key point of contact and technical expert.
+ Lead and support your team to deliver compounding, filling, lyophilization, equipment preparation, formulation, buffer preparation and processing activities in the biologics fill-finish facility to meet clearly stated operating objectives
+ Coach & mentor your manufacturing team to maximize its effectiveness through clear and effective communication
+ Promote and develop a culture of contamination control and compliance with aseptic best practices
+ Communicate departmental goals to provide cost-effective quality compliant products in a safe, effective manner
+ Collaborate with program management, supply chain, technical operations, quality, and engineering groups to ensure effective planning, scheduling and execution of commercial and NPI clinical manufacturing
+ Resolve operations/project issues with team members, project customers, and others as appropriate.
+ Drive operations excellence and key operations targets, including OEE where applicable
+ Provide direct interface as a subject matter expert with the QA department to interact with HPRA, FDA and applicable health authorities and internal audits.
Qualifications
So what will you need to be successful in this role?
Education and preferred experience:
+ Minimum of 5 years experience in batch processing, automation, commissioning, and/or validation in an FDA/HHPRA-regulated industry.
+ Bachelor's degree in chemistry, pharmacy, engineering or a related scientific field is required; an advanced degree is preferred.
+ Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
+ Comprehensive understanding of contamination control principles and regulatory expectations for aseptic processing.
+ Technical background in pharmaceutical, biologics, or similar industries.
+ A minimum of 1 year of direct supervisory experience in a team environment is preferred
+ Possess strong technical knowledge and application of concepts, practices, and procedures. Works on problems of complex scope where analysis of situations or data involves multiple competing factors. Exercises judgment and advises the appropriate actions
Additional Information
All your information will be kept confidential according to EEO guidelines.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
This advertiser has chosen not to accept applicants from your region.
4
Manufacturing Technicians / Technical Shift Leads / Technical Writers
Westport, Connacht
AbbVie
Posted 2 days ago
Job Viewed
Job Description
Company Description
AbbVie's mission is to discover and deliver innovative therapies and solutions that address serious diseases today and the medical challenges of tomorrow. We strive to make a remarkable impact on patients' lives across several key therapeutic areas: immunology, ophthalmology, oncology, neuroscience, and virology, as well as in aesthetic medicine with products and services from our Allergan Aesthetics portfolio. For more information about AbbVie, please visit: - Follow @abbvie on LinkedIn, X (formerly Twitter), Instagram, and YouTube.
Job Description
At AbbVie Westport, we are dedicated to improving lives through transformative medicines and innovative healthcare solutions. Our commitment to excellence is driven by our talented team, and we are thrilled to invite you to be a part of our journey.
Every day at AbbVie counts, as we harness passion and dedication to positively impact health worldwide. When you join AbbVie Westport, your efforts will directly contribute to the betterment of human health across the globe.
Our success is fueled by exceptional individuals with high-level technical capabilities and expertise, excelling in pioneering science and healthcare innovations.
Working at AbbVie Westport
As our business evolves through cutting-edge research, we are eager to engage with talented individuals ready to join us on our mission. We are currently hiring for
+ Manufacturing Technicians ( Technical Shift Leads
+ Technical Writers ( in joining us on this exciting journey? Please register, so we can keep you in mind for these opportunities.
Join us at AbbVie Westport, where your expertise and passion will help us make a meaningful impact on healthcare, both locally and globally.
Additional Information
Whatever your area of expertise-medical, regulatory, market access, human resources, legal, marketing, communications-you'll find exciting challenges and opportunities to explore new career paths at AbbVie.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
AbbVie's mission is to discover and deliver innovative therapies and solutions that address serious diseases today and the medical challenges of tomorrow. We strive to make a remarkable impact on patients' lives across several key therapeutic areas: immunology, ophthalmology, oncology, neuroscience, and virology, as well as in aesthetic medicine with products and services from our Allergan Aesthetics portfolio. For more information about AbbVie, please visit: - Follow @abbvie on LinkedIn, X (formerly Twitter), Instagram, and YouTube.
Job Description
At AbbVie Westport, we are dedicated to improving lives through transformative medicines and innovative healthcare solutions. Our commitment to excellence is driven by our talented team, and we are thrilled to invite you to be a part of our journey.
Every day at AbbVie counts, as we harness passion and dedication to positively impact health worldwide. When you join AbbVie Westport, your efforts will directly contribute to the betterment of human health across the globe.
Our success is fueled by exceptional individuals with high-level technical capabilities and expertise, excelling in pioneering science and healthcare innovations.
Working at AbbVie Westport
As our business evolves through cutting-edge research, we are eager to engage with talented individuals ready to join us on our mission. We are currently hiring for
+ Manufacturing Technicians ( Technical Shift Leads
+ Technical Writers ( in joining us on this exciting journey? Please register, so we can keep you in mind for these opportunities.
Join us at AbbVie Westport, where your expertise and passion will help us make a meaningful impact on healthcare, both locally and globally.
Additional Information
Whatever your area of expertise-medical, regulatory, market access, human resources, legal, marketing, communications-you'll find exciting challenges and opportunities to explore new career paths at AbbVie.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
This advertiser has chosen not to accept applicants from your region.
5
Senior Manager, Quality Control Laboratory
Westport, Connacht
AbbVie
Posted 2 days ago
Job Viewed
Job Description
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are currently looking for a Senior Manager of Quality Control Laboratories to join our team in Westport on a 12-month fixed-term contract. The Senior Manager of Quality Control is responsible for strategy, planning, and management of laboratory operations, ensuring compliance with FDA, HPRA, and EPA safety standards and budgetary constraints. This role supports the QA site head in achieving operational goals.
Responsibilities:
+ Manage and motivate employees, ensuring capacity aligns with business needs.
+ Develop and deliver business plans, manage departmental budget, and handle new product implementation.
+ Represent the company in client and regulatory meetings, ensuring GMP compliance.
+ Organize cross-functional activities to improve lab efficiencies.
+ Coordinate meetings and manage documentation and compliance tools.
Qualifications
+ Proven track record in people and operations management within Pharma/Medical Devices/Food industry.
+ Qualification in Pharmaceutical Science.
+ Excellent conflict resolution, planning, and communication skills.
+ Ability to manage in regulated environments and adapt to changes.
+ Strong commitment to AbbVie's values and business ethics.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are currently looking for a Senior Manager of Quality Control Laboratories to join our team in Westport on a 12-month fixed-term contract. The Senior Manager of Quality Control is responsible for strategy, planning, and management of laboratory operations, ensuring compliance with FDA, HPRA, and EPA safety standards and budgetary constraints. This role supports the QA site head in achieving operational goals.
Responsibilities:
+ Manage and motivate employees, ensuring capacity aligns with business needs.
+ Develop and deliver business plans, manage departmental budget, and handle new product implementation.
+ Represent the company in client and regulatory meetings, ensuring GMP compliance.
+ Organize cross-functional activities to improve lab efficiencies.
+ Coordinate meetings and manage documentation and compliance tools.
Qualifications
+ Proven track record in people and operations management within Pharma/Medical Devices/Food industry.
+ Qualification in Pharmaceutical Science.
+ Excellent conflict resolution, planning, and communication skills.
+ Ability to manage in regulated environments and adapt to changes.
+ Strong commitment to AbbVie's values and business ethics.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
This advertiser has chosen not to accept applicants from your region.
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