8 Manufacturing jobs in Westport
Manufacturing Technician
Westport, Connacht
AbbVie
Posted 3 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
There are many ways to be a difference maker. Find yours.
We are now recruiting for Manufacturing Technicians to join our diverse Biologics team in Westport, on an initial 12 months fixed-term contract basis. As our newest technician, you will ensure the highest quality and safety compliance standards while gaining exposure to new and advanced technology in our quality assurance systems. You will also ensure the continued success of our business unit by taking ownership of duties such as compounding, filling and capping of an aseptic product, preparing autoclave loads, testing filters, preparing components, documenting batch related activities, housekeeping and environmental monitoring.
PLEASE NOTE: The following role is a 12 hour monthly rotational shift pattern, covering days, nights, weekdays and weekends.
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.
Your Key Activities will include, but are not limited to:
+ Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system
+ Perform activities associated with the compounding, filling and capping of an aseptic process.
+ Prepare components and equipment for processing into a Grade A environment.
+ Accurately completing documentation on time, accurately and legibly.
+ Keeping the Manufacturing area tidy and clean.
+ Review and update documentation as requested by the Production Manager
+ Participating in root cause analysis and problem-solving.
+ Completing compliant investigations and environmental excursions.
+ Adhering to all company standards in the area of safety, housekeeping and quality, notifying management of any discrepancies.
+ Follow gowning procedures on entry to areas
+ Report any machine issues to the Production Manager and the maintenance department.
+ Set-up, clean and maintain equipment
+ Transfer of waste material out of the cleanroom areas
+ Perform environmental monitoring
+ Participate in media runs
+ Adhere to and support all EHS & E standards, procedures, and policies.
Qualifications
Education and Experience:
+ Leaving cert or equivalent qualification required, 3rd level qualification in a Science/Engineering or related discipline is preferred
+ 1-2 years GMP experience, preferably Aseptic/Sterile Manufacturing in a cleanroom environment
+ Experience working with SAP within a similar industry is preferable.
+ Strong communication, documentation, and IT skills.
+ Ability to multitask and adapt in a fast-paced environment.
+ Outstanding organization, flexibility, and time management skills
+ High attention to detail and methodical in approach
+ Ability to build strong relationships and work within cross-functional teams.
+ Adaptability to work in a fast, dynamic environment whilst adjusting readily to meet unexpected constraints.
+ Drive, high energy, maturity, and ability to work under pressure, deliver results, and overcome obstacles.
+ Team player who can collaborate with others to achieve organizational targets and goals.
So, does this all sound like the right role for you?
Then apply now and join AbbVie today!
#Monster
Additional Information
Multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&I) - a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect.
At AbbVie, your individual contributions count - help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV - we will discuss everything else with you in person.
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
There are many ways to be a difference maker. Find yours.
We are now recruiting for Manufacturing Technicians to join our diverse Biologics team in Westport, on an initial 12 months fixed-term contract basis. As our newest technician, you will ensure the highest quality and safety compliance standards while gaining exposure to new and advanced technology in our quality assurance systems. You will also ensure the continued success of our business unit by taking ownership of duties such as compounding, filling and capping of an aseptic product, preparing autoclave loads, testing filters, preparing components, documenting batch related activities, housekeeping and environmental monitoring.
PLEASE NOTE: The following role is a 12 hour monthly rotational shift pattern, covering days, nights, weekdays and weekends.
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.
Your Key Activities will include, but are not limited to:
+ Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system
+ Perform activities associated with the compounding, filling and capping of an aseptic process.
+ Prepare components and equipment for processing into a Grade A environment.
+ Accurately completing documentation on time, accurately and legibly.
+ Keeping the Manufacturing area tidy and clean.
+ Review and update documentation as requested by the Production Manager
+ Participating in root cause analysis and problem-solving.
+ Completing compliant investigations and environmental excursions.
+ Adhering to all company standards in the area of safety, housekeeping and quality, notifying management of any discrepancies.
+ Follow gowning procedures on entry to areas
+ Report any machine issues to the Production Manager and the maintenance department.
+ Set-up, clean and maintain equipment
+ Transfer of waste material out of the cleanroom areas
+ Perform environmental monitoring
+ Participate in media runs
+ Adhere to and support all EHS & E standards, procedures, and policies.
Qualifications
Education and Experience:
+ Leaving cert or equivalent qualification required, 3rd level qualification in a Science/Engineering or related discipline is preferred
+ 1-2 years GMP experience, preferably Aseptic/Sterile Manufacturing in a cleanroom environment
+ Experience working with SAP within a similar industry is preferable.
+ Strong communication, documentation, and IT skills.
+ Ability to multitask and adapt in a fast-paced environment.
+ Outstanding organization, flexibility, and time management skills
+ High attention to detail and methodical in approach
+ Ability to build strong relationships and work within cross-functional teams.
+ Adaptability to work in a fast, dynamic environment whilst adjusting readily to meet unexpected constraints.
+ Drive, high energy, maturity, and ability to work under pressure, deliver results, and overcome obstacles.
+ Team player who can collaborate with others to achieve organizational targets and goals.
So, does this all sound like the right role for you?
Then apply now and join AbbVie today!
#Monster
Additional Information
Multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&I) - a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect.
At AbbVie, your individual contributions count - help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV - we will discuss everything else with you in person.
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
Manufacturing Analyst
Westport, Connacht
AbbVie
Posted 3 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 Analyst to join our newly formed Central Cervices Team in AbbVie Westport, Co Mayo on an initial 12 months fixed term contract.
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 be actively involved and manage the batch related CAPA's as they arise in the business unit taking them from the initial review state through RCA, approval, batch disposition and delivery of corrective and preventive actions, liaising closely with the relevant Departments and QA Lead to ensure thorough investigations are complete in a timely manner.
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:
+ Use and maintenance of data within key systems such as SAP, S4HANA, Global Trackwise, POMs, One Track, One Vault and Compliance wire.
+ Document retrieval from local files and archives, as required for submissions, customer requests and others.
+ Tracking and Analysis of EM trends within the Eyecare Business Unit
+ Management of training curriculum for all using eLMS
+ Participate in and lead non-conformance and exception investigations as necessary.
+ Complete manufacturing investigations for LIRs.
+ Open and lead change control records using One Track.
+ Work with QA Teams to align and promote awareness on data integrity and good documentation practices.
+ Provide assistance when required at Regulatory Inspections.
+ Trending and co-ordination of customer complaints investigations.
+ Work close with Depts on corrective actions arising from Environmental excursions.
+ Comply with AbbVie policies and procedures and regulatory agency regulations.
Qualifications
Education and preferred experience:
+ Bachelor's degree in science, or a related field is preferred and/or a minimum of 2 years' experience in a similar role.
+ Detailed knowledge of CGMP and aseptic practices, data integrity requirements and GDP is required for this role.
+ Strong organizational skills and attention to detail are essential for this role.
+ Good interpersonal relations/communications skills
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 Analyst to join our newly formed Central Cervices Team in AbbVie Westport, Co Mayo on an initial 12 months fixed term contract.
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 be actively involved and manage the batch related CAPA's as they arise in the business unit taking them from the initial review state through RCA, approval, batch disposition and delivery of corrective and preventive actions, liaising closely with the relevant Departments and QA Lead to ensure thorough investigations are complete in a timely manner.
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:
+ Use and maintenance of data within key systems such as SAP, S4HANA, Global Trackwise, POMs, One Track, One Vault and Compliance wire.
+ Document retrieval from local files and archives, as required for submissions, customer requests and others.
+ Tracking and Analysis of EM trends within the Eyecare Business Unit
+ Management of training curriculum for all using eLMS
+ Participate in and lead non-conformance and exception investigations as necessary.
+ Complete manufacturing investigations for LIRs.
+ Open and lead change control records using One Track.
+ Work with QA Teams to align and promote awareness on data integrity and good documentation practices.
+ Provide assistance when required at Regulatory Inspections.
+ Trending and co-ordination of customer complaints investigations.
+ Work close with Depts on corrective actions arising from Environmental excursions.
+ Comply with AbbVie policies and procedures and regulatory agency regulations.
Qualifications
Education and preferred experience:
+ Bachelor's degree in science, or a related field is preferred and/or a minimum of 2 years' experience in a similar role.
+ Detailed knowledge of CGMP and aseptic practices, data integrity requirements and GDP is required for this role.
+ Strong organizational skills and attention to detail are essential for this role.
+ Good interpersonal relations/communications skills
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.
1
Manufacturing Shift Manager
Westport, Connacht
AbbVie
Posted 3 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
More than a job - It's a chance to make a real difference
Working at AbbVie is more than a job. It's a career with meaning. A chance to make a difference, in the world and in your life. We make sure you have everything you need to reach higher ground in your career. From growing and learning together to fostering a supportive space for you to thrive-at AbbVie and beyond
We are now recruiting Shift Manager to join our diverse Unit Dose Eyecare Manufacturing team in Westport. Flexibility around shifts is?essential?for these roles as it will include a rotational shift pattern of Days and Nights.
Is this a team you want to be part of? Then read on.
Purpose:
Lead and facilitate the safe operations of the primary container labelling process in the Unit Dose Department in line with all safety, regulatory and operational requirements. Assuring the long-term effectiveness of the team: delivering high levels of customer service, ensuring quality of product and services, complying with all regulatory requirements, achieving desired financial performance including cost reductions, and building a culture of high performance for the team
Responsibilities:
+ Act as key point of technical contact for coding and printing activities
+ On the floor Management and execution of equipment, preparation and support processing activities in the Eye Care facility to meet clearly stated operating objectives.
+ Team leadership, motivation and direction to maximize the effectiveness of your team, clearly communicating task details and goals to your team members, to allow them to work effectively.
+ Daily reporting on the status of all operations and support activities. Communicate the departmental goals, to provide cost effective quality compliant products in a safe, effective manner
+ Liaise with program management, supply chain, technical operations quality and engineering groups to ensure effective planning, scheduling and execution of commercial and clinical manufacturing/filling
+ Resolve operations/project issues by working with team members, project customers, and others as appropriate.
+ Drive operations excellences and Key operations targets including OEE where applicable.
+ Provides direct interface as a subject matter expert with QA department to interact with HPRA, FDA, applicable health authority and internal audits.
+ Develop direct reports by securing appropriate training, assigning progressively · challenging tasks and managing mid-year and annual reviews
Qualifications
+ You will have a Bachelor's degree or equivalent required in an engineering or Science related field
+ Minimum of 5 years' experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry
+ A working knowledge of safety, quality systems, and current Good Manufacturing Practices as applied to equipment and process steps in area of responsibility is required. familiarity with equipment and facilities validation
+ Must be flexible to handle multiple tasks including ability to handle pressure in a professional manner. Effectively work in a team environment. Maintain high level of energy and professionalism on the job. Build effective working relationships with customers, co-workers, cross-functioned groups, and management.
+ A minimum of 1 year direct supervisory experience in a team environment is an advantage.
+ Intermediate to High computer and MS Office skills
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
More than a job - It's a chance to make a real difference
Working at AbbVie is more than a job. It's a career with meaning. A chance to make a difference, in the world and in your life. We make sure you have everything you need to reach higher ground in your career. From growing and learning together to fostering a supportive space for you to thrive-at AbbVie and beyond
We are now recruiting Shift Manager to join our diverse Unit Dose Eyecare Manufacturing team in Westport. Flexibility around shifts is?essential?for these roles as it will include a rotational shift pattern of Days and Nights.
Is this a team you want to be part of? Then read on.
Purpose:
Lead and facilitate the safe operations of the primary container labelling process in the Unit Dose Department in line with all safety, regulatory and operational requirements. Assuring the long-term effectiveness of the team: delivering high levels of customer service, ensuring quality of product and services, complying with all regulatory requirements, achieving desired financial performance including cost reductions, and building a culture of high performance for the team
Responsibilities:
+ Act as key point of technical contact for coding and printing activities
+ On the floor Management and execution of equipment, preparation and support processing activities in the Eye Care facility to meet clearly stated operating objectives.
+ Team leadership, motivation and direction to maximize the effectiveness of your team, clearly communicating task details and goals to your team members, to allow them to work effectively.
+ Daily reporting on the status of all operations and support activities. Communicate the departmental goals, to provide cost effective quality compliant products in a safe, effective manner
+ Liaise with program management, supply chain, technical operations quality and engineering groups to ensure effective planning, scheduling and execution of commercial and clinical manufacturing/filling
+ Resolve operations/project issues by working with team members, project customers, and others as appropriate.
+ Drive operations excellences and Key operations targets including OEE where applicable.
+ Provides direct interface as a subject matter expert with QA department to interact with HPRA, FDA, applicable health authority and internal audits.
+ Develop direct reports by securing appropriate training, assigning progressively · challenging tasks and managing mid-year and annual reviews
Qualifications
+ You will have a Bachelor's degree or equivalent required in an engineering or Science related field
+ Minimum of 5 years' experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry
+ A working knowledge of safety, quality systems, and current Good Manufacturing Practices as applied to equipment and process steps in area of responsibility is required. familiarity with equipment and facilities validation
+ Must be flexible to handle multiple tasks including ability to handle pressure in a professional manner. Effectively work in a team environment. Maintain high level of energy and professionalism on the job. Build effective working relationships with customers, co-workers, cross-functioned groups, and management.
+ A minimum of 1 year direct supervisory experience in a team environment is an advantage.
+ Intermediate to High computer and MS Office skills
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
Incoming Quality Control (IQA) Manager
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 is seeking a dedicated Incoming Quality Control (IQA) Manager on our Westport site for a 12 month fixed term contract. This role is key to managing all IQA activities to support commercial, clinical, and development efforts at our site. The position involves ensuring comprehensive support across all business units and functions, providing guidance on QA/QC activities related to incoming inspection and release of packaging and manufacturing components, and maintaining the IQA department as a centre of excellence in quality, compliance, and efficiency.
Responsibilities
+ Establish and maintain strong relationships with the Associate Director, management, colleagues, and customers, effectively articulating quality requirements.
+ Motivate and manage employees through effective communication, ensuring daily handovers and performance review meetings align with company policy.
+ Maintain capacity and handle recruitment and management of staff, focusing on coaching and development of Quality technicians to support succession planning.
+ Assess and implement changes in response to new regulatory guidance, ensuring the success of compliance initiatives to enhance site quality programs.
+ Represent the company during Ministry of Health inspections and manage departmental budgets and headcount needs.
+ Oversee Non-conforming KPIs and maintain visibility on QMS records and compliance wire, staying updated on new inspection technologies and regulatory guidance.
+ Oversee the strategy, planning, and management of all incoming inspections, releases, and resolution of component queries in the IQA department.
+ Ensure equipment in all IQA areas is in good repair and maintain awareness of industry regulations and best practices.
+ Coordinate and schedule the IQA 1st shift, collaborating with the Associate Director to meet company goals and regulatory obligations.
Qualifications
+ Proven experience in quality control management, specifically within the pharmaceutical industry.
+ Strong technical, organisational, and people management skills with a track record of driving quality, compliance, and efficiency.
+ Expertise in IQA activities, including incoming inspection, release, retention, stock management, and file issuance.
+ Comprehensive knowledge of industry regulations and best practices, with experience supporting regulatory compliance and site audits.
+ Effective communication skills, with the ability to manage and motivate a team, articulate quality requirements, and interact with regulatory bodies.
+ Demonstrated ability to manage departmental budgets, assess regulatory changes, and develop strategic plans for quality enhancements
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 is seeking a dedicated Incoming Quality Control (IQA) Manager on our Westport site for a 12 month fixed term contract. This role is key to managing all IQA activities to support commercial, clinical, and development efforts at our site. The position involves ensuring comprehensive support across all business units and functions, providing guidance on QA/QC activities related to incoming inspection and release of packaging and manufacturing components, and maintaining the IQA department as a centre of excellence in quality, compliance, and efficiency.
Responsibilities
+ Establish and maintain strong relationships with the Associate Director, management, colleagues, and customers, effectively articulating quality requirements.
+ Motivate and manage employees through effective communication, ensuring daily handovers and performance review meetings align with company policy.
+ Maintain capacity and handle recruitment and management of staff, focusing on coaching and development of Quality technicians to support succession planning.
+ Assess and implement changes in response to new regulatory guidance, ensuring the success of compliance initiatives to enhance site quality programs.
+ Represent the company during Ministry of Health inspections and manage departmental budgets and headcount needs.
+ Oversee Non-conforming KPIs and maintain visibility on QMS records and compliance wire, staying updated on new inspection technologies and regulatory guidance.
+ Oversee the strategy, planning, and management of all incoming inspections, releases, and resolution of component queries in the IQA department.
+ Ensure equipment in all IQA areas is in good repair and maintain awareness of industry regulations and best practices.
+ Coordinate and schedule the IQA 1st shift, collaborating with the Associate Director to meet company goals and regulatory obligations.
Qualifications
+ Proven experience in quality control management, specifically within the pharmaceutical industry.
+ Strong technical, organisational, and people management skills with a track record of driving quality, compliance, and efficiency.
+ Expertise in IQA activities, including incoming inspection, release, retention, stock management, and file issuance.
+ Comprehensive knowledge of industry regulations and best practices, with experience supporting regulatory compliance and site audits.
+ Effective communication skills, with the ability to manage and motivate a team, articulate quality requirements, and interact with regulatory bodies.
+ Demonstrated ability to manage departmental budgets, assess regulatory changes, and develop strategic plans for quality enhancements
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.
3
Manufacturing Shift Manager - Biologics
Westport, Connacht
AbbVie
Posted 3 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.
4
Head of Manufacturing Services
Shannon, Munster
Ei Electronics GmbH
Posted 2 days ago
Job Viewed
Job Description
Employing over 1250 people worldwide, Ei Electronics is headquartered in Shannon, Ireland, occupying a campus where all key manufacturing, R&D and commercial functions are located. Overseas sales and marketing subsidiaries are located in the UK, Germany, France and the USA.
The Company's success is based on a culture of Quality, Service and Product Innovation over 30 years. R&D is the lifeblood of Ei Electronics, with sensor technologies at the core of our product advancement. As a global leader in the industry, Ei Electronics is now at the forefront of emerging Cloud-based "Connected Home" and IOT developments.
Working with one of Irelands leading indigenous electronics companies, provides a wide array of opportunities and possibilities to grow.
The Role ProfileWe are seeking an ambitious and driven professional to effectively lead within a fast-paced and dynamic environment. The successful candidate will be a key member of the management team within Ei and play a key role in contributing to the success of the business.
This is a unique opportunity for a Senior Manufacturing Services Manager to contribute to the ongoing operational efficiency of the key manufacturing services centres that support the final assembly operations.
Responsibilities involve coordinating and managing various manufacturing support and supply services such as molding operations, Surface Mount Assembly operations and overseeing facilities Operations to ensure continued effective management of efficiency, quality, cost, H&S and technological integration.
- Production Capacity Planning: Planning production capacity and workflows to optimize resources and meet projected output targets. Oversee, plan, organize, and direct day-to-day operations of molding and surface mount assembly operations through relevant managers and supervisors. Provide a Leadership role in the operational management of the Plant playing a key role in the delivery of the core Plant KPIs. Implement strategic initiatives in line with the company's overall targets & objectives and provide a clear sense of direction and focus to the production team.
- Quality Control: Implement and oversee quality control processes to meet company standards and customer expectations. Implement and manage programs to monitor production outputs for defects, PPM levels, 6's and Yields.
- Cost Management: Manage production costs to ensure that the manufacturing processes remain within budget. This involves monitoring expenses related to labor, materials, and overhead costs.
- Process Improvement: Continuous improvements of all key aspects of the manufacturing services support. Work on identifying areas for improvement in processes, equipment, and workflows to enhance efficiency, reduce waste, and increase productivity.
- Team Management and development: Managing and leading a team of technical staff is a significant part of the role. This includes hiring, training, and supervising staff, as well as fostering a positive work environment.
- Health and Safety: Implement and enforce safety protocols to prevent accidents and injuries. Work closely with safety officers and compliance teams to ensure support services and plant facilities are working to the highest standards possible and providing employees with a safe and healthy working environment.
- Sustainability: Provide a leadership role in managing and leading key sustainability initiative plant wide to ensure the company meets its net carbon neutral targets by 2030. Including compliance with ISO50001.
- Technology Integration: Keeping abreast of technological advancements in manufacturing is essential. Implementing new technologies and automation to improve efficiency and reduce costs is a key element of this.
- At least 7 years of operational experience, preferably at a technical management level, within a team-based operational environment. Experience in a manufacturing environment is desirable.
- Degree in Engineering (Mechanical, Production, or related field) or equivalent.
- Excellent team player with the ability to leverage the abilities of all personnel within the business unit.
- Competent in preparing business strategies and implementing action plans.
- Demonstrated experience in leading and managing technical teams.
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
Interested candidates are encouraged to submit their CV and a cover letter outlining their suitability for the role to
Ei Electronics is an equal opportunity employer and is committed to fostering an inclusive and diverse workplace.
This advertiser has chosen not to accept applicants from your region.
5
Biologics (Manufacturing) Technical Shift Lead
Westport, Connacht
AbbVie
Posted 3 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.
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6
Manufacturing Technicians / Technical Shift Leads / Technical Writers
Westport, Connacht
AbbVie
Posted 3 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.
7