154 Manufacturing Processes jobs in Ireland
Quality Control Student
Wicklow, Leinster
Takeda Pharmaceuticals
Posted today
Job Viewed
Job Description
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
Are you looking for a patient-oriented, innovation-driven company that inspires you and promotes your career? Then take your future in your hands and become part of Takeda as a
**_Quality Control Student_**
This role offers a unique opportunity to gain hands-on experience with cutting-edge analytical techniques in a dynamic, supportive team at Takeda's world-class facilities in Bray. Join us to develop your skills, contribute to life-changing medicines, and grow your career in an environment that values innovation, safety, and personal development.
**_How you will contribute:_**
+ To observe GLP/cGMP at all times.
+ Testing of all laboratory samples including Raw Materials, Packaging Components, Product Validation, Stability, Environmental and OH.
+ Performance of laboratory tests as per written procedure or as per pharmacopoeia.
+ Recording of analytical results accurately.
+ Operation, maintenance and calibration of laboratory instruments.
+ To maintain written training records.
+ To ensure that the laboratory is kept clean, tidy and safe at all times.
In this position you will report to the **Quality Control Team Leader** .
**_What you bring to Takeda:_**
+ Participate fully in any cross functional training initiatives.
+ Drive and promote the corporate values of Takeda-ism within the workplace.
+ Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business.
+ Ensure that Accident Reports / Near Miss Forms are completed in a timely manner after an event.
+ Ensure timely completion of all SOP, reading, training and assessment.
+ Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.
+ Is adaptable to changing priorities.
**_What Takeda can offer you:_**
+ Flexible working arrangements
+ 26 vacation days plus additional days for service milestones
+ Employee Assistance Program
+ Wellbeing and engagement teams
+ Development opportunities
+ Coaching and mentoring
+ Humanitarian volunteering leave options
+ Subsidized canteen
+ Electric charging points available at parking locations
**_More about us:_**
Takeda is focused on creating better health for people and a brighter future for the world. We aim to discover and deliver life-transforming treatments in our core therapeutic and business areas, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines.
Takeda Ireland was established in 1997. Our story in Ireland is one of substantial growth, rapid change, and innovation. Over the past years, Takeda Ireland has invested over 55 million in Ireland to develop our manufacturing sites. Solidifying our commitment in our people and contributing to the local economy. Takeda in Ireland has commercial operations, corporate services, and manufacturing facilities across four locations: Baggot St, Bray, Citywest, and Grange Castle. We have been certified as Top Employer for several consecutive years.
**_How we will support you:_**
Takeda is proud of its commitment to create a diverse workforce and to provide equal employment opportunities to all employees and applicants for employment without regard to ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status or any other characteristic protected by law. If you are living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process.
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time
**Job Description**
Are you looking for a patient-oriented, innovation-driven company that inspires you and promotes your career? Then take your future in your hands and become part of Takeda as a
**_Quality Control Student_**
This role offers a unique opportunity to gain hands-on experience with cutting-edge analytical techniques in a dynamic, supportive team at Takeda's world-class facilities in Bray. Join us to develop your skills, contribute to life-changing medicines, and grow your career in an environment that values innovation, safety, and personal development.
**_How you will contribute:_**
+ To observe GLP/cGMP at all times.
+ Testing of all laboratory samples including Raw Materials, Packaging Components, Product Validation, Stability, Environmental and OH.
+ Performance of laboratory tests as per written procedure or as per pharmacopoeia.
+ Recording of analytical results accurately.
+ Operation, maintenance and calibration of laboratory instruments.
+ To maintain written training records.
+ To ensure that the laboratory is kept clean, tidy and safe at all times.
In this position you will report to the **Quality Control Team Leader** .
**_What you bring to Takeda:_**
+ Participate fully in any cross functional training initiatives.
+ Drive and promote the corporate values of Takeda-ism within the workplace.
+ Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business.
+ Ensure that Accident Reports / Near Miss Forms are completed in a timely manner after an event.
+ Ensure timely completion of all SOP, reading, training and assessment.
+ Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.
+ Is adaptable to changing priorities.
**_What Takeda can offer you:_**
+ Flexible working arrangements
+ 26 vacation days plus additional days for service milestones
+ Employee Assistance Program
+ Wellbeing and engagement teams
+ Development opportunities
+ Coaching and mentoring
+ Humanitarian volunteering leave options
+ Subsidized canteen
+ Electric charging points available at parking locations
**_More about us:_**
Takeda is focused on creating better health for people and a brighter future for the world. We aim to discover and deliver life-transforming treatments in our core therapeutic and business areas, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines.
Takeda Ireland was established in 1997. Our story in Ireland is one of substantial growth, rapid change, and innovation. Over the past years, Takeda Ireland has invested over 55 million in Ireland to develop our manufacturing sites. Solidifying our commitment in our people and contributing to the local economy. Takeda in Ireland has commercial operations, corporate services, and manufacturing facilities across four locations: Baggot St, Bray, Citywest, and Grange Castle. We have been certified as Top Employer for several consecutive years.
**_How we will support you:_**
Takeda is proud of its commitment to create a diverse workforce and to provide equal employment opportunities to all employees and applicants for employment without regard to ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status or any other characteristic protected by law. If you are living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process.
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time
This advertiser has chosen not to accept applicants from your region.
0
Quality Control Student
Dublin, Leinster
Takeda Pharmaceuticals
Posted today
Job Viewed
Job Description
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
Are you looking for a patient-oriented, innovation-driven company that inspires you and promotes your career? Then take your future in your hands and become part of Takeda as a
**_Quality Control Student_**
This role offers a unique opportunity to gain hands-on experience with cutting-edge analytical techniques in a dynamic, supportive team at Takeda's world-class facilities in Grange Castle. Join us to develop your skills, contribute to life-changing medicines, and grow your career in an environment that values innovation, safety, and personal development.
**How you will contribute:**
+ Apply your knowledge of analytical techniques (such as HPLC, GC, wet chemistry) to perform accurate testing of samples and materials.
+ Participate in calibration and maintenance of laboratory equipment to ensure reliable and compliant operations.
+ Support a safe, clean, and efficient laboratory environment by adhering to 5S practices and all safety procedures.
+ Engage in cross-functional training and contribute to QC improvement projects, enhancing both your skills and team performance.
+ Demonstrate strong organizational, communication, and report writing abilities while working within a collaborative team.
+ Champion Takeda-ism values every day, fostering innovation, integrity, and continuous improvement in our Grange Castle site.
In this position you will report to the (insert job title of the supervisor, not the name).
**What you bring to Takeda:**
+ Solid foundational knowledge in analytical techniques, including HPLC, GC, and wet chemistry, gained through your degree studies.
+ Practical experience handling laboratory tasks and equipment, demonstrating attention to detail and compliance with quality standards.
+ Strong organizational skills and the ability to manage multiple priorities in a fast-paced environment.
+ Effective communication and interpersonal abilities to support teamwork and clear reporting.
+ Proficiency with Microsoft Office and digital tools to efficiently document and analyse laboratory data.
**What Takeda can offer you:**
+ Flexible working arrangements
+ 26 vacation days plus additional days for service milestones
+ Employee Assistance Program
+ Wellbeing and engagement teams
+ Development opportunities
+ Coaching and mentoring
+ Humanitarian volunteering leave options
+ Subsidized canteen
+ Electric charging points available at parking locations
**More about us:**
Takeda is focused on creating better health for people and a brighter future for the world. We aim to discover and deliver life-transforming treatments in our core therapeutic and business areas, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines.
Takeda Ireland was established in 1997. Our story in Ireland is one of substantial growth, rapid change, and innovation. Over the past years, Takeda Ireland has invested over 55 million in Ireland to develop our manufacturing sites. Solidifying our commitment in our people and contributing to the local economy. Takeda in Ireland has commercial operations, corporate services, and manufacturing facilities across four locations: Baggot St, Bray, Citywest, and Grange Castle. We have been certified as Top Employer for several consecutive years.
**How we will support you:**
Takeda is proud of its commitment to create a diverse workforce and to provide equal employment opportunities to all employees and applicants for employment without regard to ethnicity, colour, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status or any other characteristic protected by law. If you are living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process.
**Locations**
Grange Castle, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time
**Job Description**
Are you looking for a patient-oriented, innovation-driven company that inspires you and promotes your career? Then take your future in your hands and become part of Takeda as a
**_Quality Control Student_**
This role offers a unique opportunity to gain hands-on experience with cutting-edge analytical techniques in a dynamic, supportive team at Takeda's world-class facilities in Grange Castle. Join us to develop your skills, contribute to life-changing medicines, and grow your career in an environment that values innovation, safety, and personal development.
**How you will contribute:**
+ Apply your knowledge of analytical techniques (such as HPLC, GC, wet chemistry) to perform accurate testing of samples and materials.
+ Participate in calibration and maintenance of laboratory equipment to ensure reliable and compliant operations.
+ Support a safe, clean, and efficient laboratory environment by adhering to 5S practices and all safety procedures.
+ Engage in cross-functional training and contribute to QC improvement projects, enhancing both your skills and team performance.
+ Demonstrate strong organizational, communication, and report writing abilities while working within a collaborative team.
+ Champion Takeda-ism values every day, fostering innovation, integrity, and continuous improvement in our Grange Castle site.
In this position you will report to the (insert job title of the supervisor, not the name).
**What you bring to Takeda:**
+ Solid foundational knowledge in analytical techniques, including HPLC, GC, and wet chemistry, gained through your degree studies.
+ Practical experience handling laboratory tasks and equipment, demonstrating attention to detail and compliance with quality standards.
+ Strong organizational skills and the ability to manage multiple priorities in a fast-paced environment.
+ Effective communication and interpersonal abilities to support teamwork and clear reporting.
+ Proficiency with Microsoft Office and digital tools to efficiently document and analyse laboratory data.
**What Takeda can offer you:**
+ Flexible working arrangements
+ 26 vacation days plus additional days for service milestones
+ Employee Assistance Program
+ Wellbeing and engagement teams
+ Development opportunities
+ Coaching and mentoring
+ Humanitarian volunteering leave options
+ Subsidized canteen
+ Electric charging points available at parking locations
**More about us:**
Takeda is focused on creating better health for people and a brighter future for the world. We aim to discover and deliver life-transforming treatments in our core therapeutic and business areas, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines.
Takeda Ireland was established in 1997. Our story in Ireland is one of substantial growth, rapid change, and innovation. Over the past years, Takeda Ireland has invested over 55 million in Ireland to develop our manufacturing sites. Solidifying our commitment in our people and contributing to the local economy. Takeda in Ireland has commercial operations, corporate services, and manufacturing facilities across four locations: Baggot St, Bray, Citywest, and Grange Castle. We have been certified as Top Employer for several consecutive years.
**How we will support you:**
Takeda is proud of its commitment to create a diverse workforce and to provide equal employment opportunities to all employees and applicants for employment without regard to ethnicity, colour, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status or any other characteristic protected by law. If you are living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process.
**Locations**
Grange Castle, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time
This advertiser has chosen not to accept applicants from your region.
1
Quality Control Analyst
Dublin, Leinster
AbbVie
Posted today
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 QC Analyst at our manufacturing site in North Dublin
The QC Analyst is responsible for conducting raw material, in process, finished product and stability testing according to relevant SOPs and in adherence to the site production schedule and for accurately completing all documentation that supports testing procedures. The QC Analyst identifies issues related to laboratory testing and equipment that requires an in-depth knowledge of scientific methods and techniques. The QC Analyst is responsible for the safe, compliant, and efficient execution of job duties in a team environment. This position reports to the QC Supervisor.
Primary duties and responsibilities of the position are as follows
+ Conduct chemical and physical laboratory tests and analyze excipients, cleaning samples, raw materials, intermediates, and final products including protocol testing in a timely manner to ensure compliance with standards and production targets.
+ Recognize and report to immediate supervisor any issues or deviations from accepted standards.
+ Provide status updates on own activities and productivity challenges according to defined procedures
+ Maintain data integrity and ensure compliance with FDA, GLP, QSR and cGMP regulations, as well as with company SOPs and specifications.
+ Complete and conform to all training requirements for job role, including company-required and job role-specific training.
+ Observe all safety and compliance procedures and actively highlighting any safety concerns to help drive the reduction of accidents or near misses.
+ Conforming to the safety culture on site on Zero, Believe it, Achieve it.
+ Participate in the 6S activities within the QC Laboratory.
+ Positively contribute to departmental goals and programs such as Right First Time
Qualifications
+ A third level qualification in Chemistry or related Science, preferably a Bachelor's Degree
+ Demonstrate knowledge of cGMP requirements and practices including knowledge of the USP and FDA
+ Guidance Documents relating to the pharmaceutical Quality Control Laboratory.
+ Demonstrate knowledge of common analytical instrumentation e.g. HPLC, Dissolution, GC, FTIR, Electro Chemistry (DME), UV/Vis and other USP instrumental and Wet chemistry technologies used in pharmaceutical Quality Control Laboratory.
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 QC Analyst at our manufacturing site in North Dublin
The QC Analyst is responsible for conducting raw material, in process, finished product and stability testing according to relevant SOPs and in adherence to the site production schedule and for accurately completing all documentation that supports testing procedures. The QC Analyst identifies issues related to laboratory testing and equipment that requires an in-depth knowledge of scientific methods and techniques. The QC Analyst is responsible for the safe, compliant, and efficient execution of job duties in a team environment. This position reports to the QC Supervisor.
Primary duties and responsibilities of the position are as follows
+ Conduct chemical and physical laboratory tests and analyze excipients, cleaning samples, raw materials, intermediates, and final products including protocol testing in a timely manner to ensure compliance with standards and production targets.
+ Recognize and report to immediate supervisor any issues or deviations from accepted standards.
+ Provide status updates on own activities and productivity challenges according to defined procedures
+ Maintain data integrity and ensure compliance with FDA, GLP, QSR and cGMP regulations, as well as with company SOPs and specifications.
+ Complete and conform to all training requirements for job role, including company-required and job role-specific training.
+ Observe all safety and compliance procedures and actively highlighting any safety concerns to help drive the reduction of accidents or near misses.
+ Conforming to the safety culture on site on Zero, Believe it, Achieve it.
+ Participate in the 6S activities within the QC Laboratory.
+ Positively contribute to departmental goals and programs such as Right First Time
Qualifications
+ A third level qualification in Chemistry or related Science, preferably a Bachelor's Degree
+ Demonstrate knowledge of cGMP requirements and practices including knowledge of the USP and FDA
+ Guidance Documents relating to the pharmaceutical Quality Control Laboratory.
+ Demonstrate knowledge of common analytical instrumentation e.g. HPLC, Dissolution, GC, FTIR, Electro Chemistry (DME), UV/Vis and other USP instrumental and Wet chemistry technologies used in pharmaceutical Quality Control Laboratory.
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
Manager, Quality Control
Sligo, Connacht
AbbVie
Posted today
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 QC Manager to join our team on our Manorhamilton Road site in Sligo. The QC Lab Manager is integral to managing a team responsible for QC testing, ensuring adherence to product specifications, quality, and safety goals. This role involves overseeing laboratory operations, including analytical testing for API and OSD products, and coordinating with internal teams to meet testing schedules.
Responsibilities:
+ Manage a lab team performing QC testing, ensuring compliance with data integrity policies and regulatory requirements.
+ Conduct and supervise all aspects of API and OSD analytical testing.
+ Ensure timely sampling, inspection, and testing, coordinating with teams for schedules and priorities.
+ Participate in internal and external audits and address audit findings.
+ Prepare technical reports, lead investigations, and implement CAPAs.
+ Provide training and support to lab team to achieve daily and long-term goals.
+ Present technical data to stakeholders to facilitate prompt decision-making.
+ Report to the Senior QC Manager.
Qualifications
+ M.Sc./B.Sc. in Chemistry or a related discipline.
+ Minimum 4 years of experience in people management within a pharmaceutical lab setting.
+ Strong knowledge of QA/QC operations, analytical testing for API and OSD.
+ Excellent presentation and technical report writing skills.
+ Strong communication and interpersonal skills, with a commitment to quality and compliance.
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 QC Manager to join our team on our Manorhamilton Road site in Sligo. The QC Lab Manager is integral to managing a team responsible for QC testing, ensuring adherence to product specifications, quality, and safety goals. This role involves overseeing laboratory operations, including analytical testing for API and OSD products, and coordinating with internal teams to meet testing schedules.
Responsibilities:
+ Manage a lab team performing QC testing, ensuring compliance with data integrity policies and regulatory requirements.
+ Conduct and supervise all aspects of API and OSD analytical testing.
+ Ensure timely sampling, inspection, and testing, coordinating with teams for schedules and priorities.
+ Participate in internal and external audits and address audit findings.
+ Prepare technical reports, lead investigations, and implement CAPAs.
+ Provide training and support to lab team to achieve daily and long-term goals.
+ Present technical data to stakeholders to facilitate prompt decision-making.
+ Report to the Senior QC Manager.
Qualifications
+ M.Sc./B.Sc. in Chemistry or a related discipline.
+ Minimum 4 years of experience in people management within a pharmaceutical lab setting.
+ Strong knowledge of QA/QC operations, analytical testing for API and OSD.
+ Excellent presentation and technical report writing skills.
+ Strong communication and interpersonal skills, with a commitment to quality and compliance.
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
2026 Graduate Quality Control Analyst
Ringaskiddy, Munster
J&J Family of Companies
Posted today
Job Viewed
Job Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
Quality
**Job Sub** **Function:**
Quality Control
**Job Category:**
Professional
**All Job Posting Locations:**
Ringaskiddy, Cork, Ireland
**Job Description:**
**Position:** Graduate Quality Control Analyst
**Start Date:** September 2026
**Location:** Cork, Ireland
**Johnson & Johnson Innovative Medicine** established its operation in Ringaskiddy in 2005 on a 100-acre site with an investment of 500 million. For more than 25 years we have been a global leader in the field of biomedicines, particularly in groundbreaking monoclonal antibody technology, an approach to producing medicines that launched a new generation of products to treat immune related diseases such as rheumatoid arthritis and plaque psoriasis.
The facility in Ringaskiddy is fully operational and currently expanding its operations to continue focusing on producing biomedicines for both the treatment of immune related diseases and new and creative cancer treatments.
**ABOUT THE JOHNSON & JOHNSON GRADUATE PROGRAMME**
The Graduate Programme is a collaborative programme across the Johnson & Johnson Campus Ireland Sites. It is aimed at high potential individuals who, when given the right tools, are empowered to proactively take responsibility, effect change and make a positive contribution to their teams and the business.
**THE SUCCESSFUL CANDIDATE WILL HAVE THE OPPORTUNITY TO:**
+ Develop relevant technical skills within their area of expertise.
+ Experience cross functional exposure both on site and within Campus Ireland.
+ Participate in regular one to ones and feedback to support your on-going development.
+ Engage in personal development and effectiveness training.
+ Develop influencing & communication skills.
+ Gain Project Management experience.
+ Learn new and innovative technologies.
+ Gain exposure to Senior Management Team.
+ Participate in continuous professional development program with a recognised qualification.
**JOB PURPOSE:**
We have an exciting opportunity for a QC Analyst on the Ireland Graduate Program. This individual will be responsible for carrying out tasks and projects related to the analysis of biotechnology products as required by Good Manufacturing practice (GMP). The individual will participate in the delivery of lab testing efforts by using both existing and new procedures or processes to independently interpret data and identify and correct issues. Proposes ideas and next steps to supervisors and/or managers. Receives intermittent, moderately detailed instructions from Quality leaders at various levels, in addition to other partners.
**WHAT YOU'RE GREAT AT:**
+ Analytical testing knowledge including an understanding of Biopharmaceutical manufacturing and batch release processes.
+ Knowledge of equipment qualification, analytical method transfers, root cause problem solving and continuous improvement desirable.
+ A strong teammate who is very customer focused, possesses leadership and testing skills and both stakeholder and project management experience.
+ Strong collaboration & interpersonal skills, both written and oral.
**AS A QC ANALYST YOUR TYPICAL DAY MAY INCLUDE:**
+ Supporting the QC Team Leader during day to day operations of area.
+ Testing for laboratory related projects e.g. analytical method transfers, equipment qualification, invalid assay and NC reduction initiatives etc.
+ Performing IP/ Microbiology/ Bioassay/ Separations analysis.
+ Identifying and implementing laboratory process improvements leading to improved efficiency &/or compliance within area.
+ Authors and investigates internal investigations, participates in regulatory inspections & external technical discussions etc.
+ Keeping up to date with analytical technology and regulatory / compliance trends.
+ Participates in technical groups to implement laboratory activities while following local and global regulatory requirements as well as J&J standards.
+ Supports the roll-out of laboratory activities (for example, instrument life-cycle management).
+ Performs laboratory studies, projects, and processes/initiatives.
+ Assists in developing lab strategies, policies, and guidelines linked to area of expertise (for example, authoring Standard Operating Procedures).
+ Contributes to external and/or internal manuscripts, regulatory reports, and technical reports.
+ Supports equipment qualifications to ensure accuracy and consistency of results.
**QUALIFICATIONS**
**Education and Experience:**
+ Minimum Bachelors degree in Chemistry, Biochemistry or related Scientific discipline.
+ Recent graduate (2025 or due to graduate in 2026).
+ Technical troubleshooting and problem-solving skills.
+ Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals.
+ Be ambitious with excellent social, communication and partner management skills.
+ Acute attention to detail.
+ A focus on patients and customers at all times.
Quality
**Job Sub** **Function:**
Quality Control
**Job Category:**
Professional
**All Job Posting Locations:**
Ringaskiddy, Cork, Ireland
**Job Description:**
**Position:** Graduate Quality Control Analyst
**Start Date:** September 2026
**Location:** Cork, Ireland
**Johnson & Johnson Innovative Medicine** established its operation in Ringaskiddy in 2005 on a 100-acre site with an investment of 500 million. For more than 25 years we have been a global leader in the field of biomedicines, particularly in groundbreaking monoclonal antibody technology, an approach to producing medicines that launched a new generation of products to treat immune related diseases such as rheumatoid arthritis and plaque psoriasis.
The facility in Ringaskiddy is fully operational and currently expanding its operations to continue focusing on producing biomedicines for both the treatment of immune related diseases and new and creative cancer treatments.
**ABOUT THE JOHNSON & JOHNSON GRADUATE PROGRAMME**
The Graduate Programme is a collaborative programme across the Johnson & Johnson Campus Ireland Sites. It is aimed at high potential individuals who, when given the right tools, are empowered to proactively take responsibility, effect change and make a positive contribution to their teams and the business.
**THE SUCCESSFUL CANDIDATE WILL HAVE THE OPPORTUNITY TO:**
+ Develop relevant technical skills within their area of expertise.
+ Experience cross functional exposure both on site and within Campus Ireland.
+ Participate in regular one to ones and feedback to support your on-going development.
+ Engage in personal development and effectiveness training.
+ Develop influencing & communication skills.
+ Gain Project Management experience.
+ Learn new and innovative technologies.
+ Gain exposure to Senior Management Team.
+ Participate in continuous professional development program with a recognised qualification.
**JOB PURPOSE:**
We have an exciting opportunity for a QC Analyst on the Ireland Graduate Program. This individual will be responsible for carrying out tasks and projects related to the analysis of biotechnology products as required by Good Manufacturing practice (GMP). The individual will participate in the delivery of lab testing efforts by using both existing and new procedures or processes to independently interpret data and identify and correct issues. Proposes ideas and next steps to supervisors and/or managers. Receives intermittent, moderately detailed instructions from Quality leaders at various levels, in addition to other partners.
**WHAT YOU'RE GREAT AT:**
+ Analytical testing knowledge including an understanding of Biopharmaceutical manufacturing and batch release processes.
+ Knowledge of equipment qualification, analytical method transfers, root cause problem solving and continuous improvement desirable.
+ A strong teammate who is very customer focused, possesses leadership and testing skills and both stakeholder and project management experience.
+ Strong collaboration & interpersonal skills, both written and oral.
**AS A QC ANALYST YOUR TYPICAL DAY MAY INCLUDE:**
+ Supporting the QC Team Leader during day to day operations of area.
+ Testing for laboratory related projects e.g. analytical method transfers, equipment qualification, invalid assay and NC reduction initiatives etc.
+ Performing IP/ Microbiology/ Bioassay/ Separations analysis.
+ Identifying and implementing laboratory process improvements leading to improved efficiency &/or compliance within area.
+ Authors and investigates internal investigations, participates in regulatory inspections & external technical discussions etc.
+ Keeping up to date with analytical technology and regulatory / compliance trends.
+ Participates in technical groups to implement laboratory activities while following local and global regulatory requirements as well as J&J standards.
+ Supports the roll-out of laboratory activities (for example, instrument life-cycle management).
+ Performs laboratory studies, projects, and processes/initiatives.
+ Assists in developing lab strategies, policies, and guidelines linked to area of expertise (for example, authoring Standard Operating Procedures).
+ Contributes to external and/or internal manuscripts, regulatory reports, and technical reports.
+ Supports equipment qualifications to ensure accuracy and consistency of results.
**QUALIFICATIONS**
**Education and Experience:**
+ Minimum Bachelors degree in Chemistry, Biochemistry or related Scientific discipline.
+ Recent graduate (2025 or due to graduate in 2026).
+ Technical troubleshooting and problem-solving skills.
+ Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals.
+ Be ambitious with excellent social, communication and partner management skills.
+ Acute attention to detail.
+ A focus on patients and customers at all times.
This advertiser has chosen not to accept applicants from your region.
4
Chemistry Supervisor, Laboratory Quality Control
Sligo, Connacht
AbbVie
Posted today
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
Job Description
We are now hiring a QC Analytical Lab Supervisor to join our team in Abbvie Ballytivnan, Sligo. You will lead the QC Analytical team and ensure the continued success of the team. Ensure that technical and systems excellence is maintained in the laboratory by ensuring own skills are maintained, by coaching and training analysts to ensure right first-time behavior and by implementing improved working practices in terms of efficiency, compliance and Right First Time.
A snapshot of your key responsibilities:
+ Supervise Daily Laboratory operations, ensuring personnel execute their responsibilities in strict accordance with relevant regulatory guidelines. Support the weekly and daily production schedules and participate in the daily Tier 1 & 2 meeting.
+ Ensure Laboratory Documentation and Computerized Systems (LIMS, Empower, LabX) compliance with Data Integrity policies and regulatory requirements.
+ Supervise the QC Analytical laboratory operations and ensure compliance with regulations including EU Annex 1, ISO, WHO, FDA Guidelines for Aseptic Processing, among others.
+ Resolving analytical OOS issues as they arise in a timely manner both through practical work and through solTRAQs/OneTrack systems.
+ Review of results from Clean & Utilities program (WFI/RO/CS water testing), Product Testing (In process and Final product as required) and Analytical Lab (pH, TOC, Conductivity, Osmolality, Density, HPLC, Raman, etc.) activities, results and raw data on time, accurately and legibly.
+ Participate actively in Laboratory Investigations Reports (LIRs), Invalid results investigation review, approval and creation of effective CAPAs. Initiate and Collaborate with all Out of Specification (OOS) results.
+ Ensuring 6S excellence is maintained across the Laboratory.
+ Instilling a quality culture of Zero, Believe it, Achieve it amongst the QC laboratory team.
+ Lead and contribute to project initiatives to improve laboratory operations and efficiency as assigned by the QC Lab Manager, acting as designee for the Laboratory Manager as assigned.
+ Work with a cross functional team, Supervisors, Quality Manager and Laboratory Manager to ensure compliance with Quality Management System
+ Support the training and mentoring of laboratory personnel and contribute to training program development.
+ Operates in an environment which is essentially self-managed but with supervision through the Laboratory Manager.
+ Provides supervision to direct reports and be responsible for setting annual goals, completing reviews, growth plans and performance management of the team.
Qualifications
Qualifications
List required and preferred qualifications (up to 10). Include education, skills and experience.
+ BS in science or equivalent (Chemistry, Microbiology, or Biology preferred)
+ 2-5 years of laboratory experience
+ 2-5 years of supervisory experience
+ Demonstrated skills to deal effectively with members of the department and the areas serviced by the laboratory
+ Problem solving skills are required
+ Must be able to interpret impact of laboratory data for appropriate and effective actions
+ Must be able to identify problem areas requiring development, maintenance, production, engineering, accounting, or planning with assistance from more senior staff
+ Must also be able to identify, communicate, and follow-through to completion and assist in the development of necessary corrective action plans to resolve the problem with supervision. May also assist in the activities required for the investigation and resolution
Additional Information
+ 3rd Level Qualification in a Science Discipline, preferably Analytical related.
Job Technical Skills
+ Minimum 4 years experience in the pharmaceutical industry.
+ Proven track record in an analytical role. Must be expert in HPLC, Raman, pH, Osmolality, Conductivity, among others.
+ Experience with HPLC, Raman and Analytical methods (pH, TOC, Osmolality, Density, among others) preferred.
+ Experience and good knowledge of SampleManager and Empower systems.
+ Involvement in product transfers / method transfer, method development experience preferred.
+ Good knowledge and understanding of Data Integrity from Laboratory perspective.
+ Preferable knowledge in ADC (Antibody-Drug Conjugate), mAb (Monoclonal Antibodies) and Aseptic process production.
Business Skills
+ Excellent communication, organization, time-management and teamwork skills
+ Requires a high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures.
+ Requires total commitment to quality and maintaining a high standard of work at all times.
+ Demonstrate ability to work on one's own initiative.
+ Strong Problem-solving skills.
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
Job Description
We are now hiring a QC Analytical Lab Supervisor to join our team in Abbvie Ballytivnan, Sligo. You will lead the QC Analytical team and ensure the continued success of the team. Ensure that technical and systems excellence is maintained in the laboratory by ensuring own skills are maintained, by coaching and training analysts to ensure right first-time behavior and by implementing improved working practices in terms of efficiency, compliance and Right First Time.
A snapshot of your key responsibilities:
+ Supervise Daily Laboratory operations, ensuring personnel execute their responsibilities in strict accordance with relevant regulatory guidelines. Support the weekly and daily production schedules and participate in the daily Tier 1 & 2 meeting.
+ Ensure Laboratory Documentation and Computerized Systems (LIMS, Empower, LabX) compliance with Data Integrity policies and regulatory requirements.
+ Supervise the QC Analytical laboratory operations and ensure compliance with regulations including EU Annex 1, ISO, WHO, FDA Guidelines for Aseptic Processing, among others.
+ Resolving analytical OOS issues as they arise in a timely manner both through practical work and through solTRAQs/OneTrack systems.
+ Review of results from Clean & Utilities program (WFI/RO/CS water testing), Product Testing (In process and Final product as required) and Analytical Lab (pH, TOC, Conductivity, Osmolality, Density, HPLC, Raman, etc.) activities, results and raw data on time, accurately and legibly.
+ Participate actively in Laboratory Investigations Reports (LIRs), Invalid results investigation review, approval and creation of effective CAPAs. Initiate and Collaborate with all Out of Specification (OOS) results.
+ Ensuring 6S excellence is maintained across the Laboratory.
+ Instilling a quality culture of Zero, Believe it, Achieve it amongst the QC laboratory team.
+ Lead and contribute to project initiatives to improve laboratory operations and efficiency as assigned by the QC Lab Manager, acting as designee for the Laboratory Manager as assigned.
+ Work with a cross functional team, Supervisors, Quality Manager and Laboratory Manager to ensure compliance with Quality Management System
+ Support the training and mentoring of laboratory personnel and contribute to training program development.
+ Operates in an environment which is essentially self-managed but with supervision through the Laboratory Manager.
+ Provides supervision to direct reports and be responsible for setting annual goals, completing reviews, growth plans and performance management of the team.
Qualifications
Qualifications
List required and preferred qualifications (up to 10). Include education, skills and experience.
+ BS in science or equivalent (Chemistry, Microbiology, or Biology preferred)
+ 2-5 years of laboratory experience
+ 2-5 years of supervisory experience
+ Demonstrated skills to deal effectively with members of the department and the areas serviced by the laboratory
+ Problem solving skills are required
+ Must be able to interpret impact of laboratory data for appropriate and effective actions
+ Must be able to identify problem areas requiring development, maintenance, production, engineering, accounting, or planning with assistance from more senior staff
+ Must also be able to identify, communicate, and follow-through to completion and assist in the development of necessary corrective action plans to resolve the problem with supervision. May also assist in the activities required for the investigation and resolution
Additional Information
+ 3rd Level Qualification in a Science Discipline, preferably Analytical related.
Job Technical Skills
+ Minimum 4 years experience in the pharmaceutical industry.
+ Proven track record in an analytical role. Must be expert in HPLC, Raman, pH, Osmolality, Conductivity, among others.
+ Experience with HPLC, Raman and Analytical methods (pH, TOC, Osmolality, Density, among others) preferred.
+ Experience and good knowledge of SampleManager and Empower systems.
+ Involvement in product transfers / method transfer, method development experience preferred.
+ Good knowledge and understanding of Data Integrity from Laboratory perspective.
+ Preferable knowledge in ADC (Antibody-Drug Conjugate), mAb (Monoclonal Antibodies) and Aseptic process production.
Business Skills
+ Excellent communication, organization, time-management and teamwork skills
+ Requires a high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures.
+ Requires total commitment to quality and maintaining a high standard of work at all times.
+ Demonstrate ability to work on one's own initiative.
+ Strong Problem-solving skills.
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 today
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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6
Senior Associate Quality Control (Shift)
Dublin, Leinster
Life Science Recruitment Ltd
Posted today
Job Viewed
Job Description
Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Senior Associate QC will work under minimal supervision, responsible for one or more of the following activities in QC including analytical testing in process, stability, and finished products. In-depth HPLC experience with Empower Software, some protein concentration testing background with strong GMP lab environment experience. Duties: Testing of in process, stability and finished product samples. eg HPLC, CE, SDS-PAGE, IEF analytical testing, characterization and sample and data management. Review and authorisation of Lab Data Support Analytical Technical Transfer activity testing reports and documentation. Document review/updates when required. Equipment Calibration, Maintenance and Trouble Shooting. Method Validation/Verification. Training of QC Chemistry Laboratory colleagues. Laboratory Investigation support Laboratory Housekeeping and maintaining GMP standards. Assisting in regulatory audits. Education and Experience: Hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology or similar Scientific Subject. 5+ years relevant experience in a pharmaceutical/healthcare environment. Have strong technical writing skills. Be detail oriented, self-motivated with good troubleshooting and problem solving abilities. Experience with analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing would also be advantageous. If interested in this posting please feel free to contact Avishek Singh at Avishek.sing or for further information.
This advertiser has chosen not to accept applicants from your region.
7
Senior associate quality control (shift)
Dublin, Leinster
Life Science Recruitment Ltd
Posted today
Job Viewed
Job Description
Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin.
This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Senior Associate QC will work under minimal supervision, responsible for one or more of the following activities in QC including analytical testing in process, stability, and finished products.
In-depth HPLC experience with Empower Software, some protein concentration testing background with strong GMP lab environment experience.
Duties: Testing of in process, stability and finished product samples.
eg HPLC, CE, SDS-PAGE, IEF analytical testing, characterization and sample and data management.
Review and authorisation of Lab Data Support Analytical Technical Transfer activity testing reports and documentation.
Document review/updates when required.
Equipment Calibration, Maintenance and Trouble Shooting.
Method Validation/Verification.
Training of QC Chemistry Laboratory colleagues.
Laboratory Investigation support Laboratory Housekeeping and maintaining GMP standards.
Assisting in regulatory audits.
Education and Experience: Hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology or similar Scientific Subject.
5+ years relevant experience in a pharmaceutical/healthcare environment.
Have strong technical writing skills.
Be detail oriented, self-motivated with good troubleshooting and problem solving abilities.
Experience with analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing would also be advantageous.
If interested in this posting please feel free to contact Avishek Singh at Avishek.sing or for further information.
This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Senior Associate QC will work under minimal supervision, responsible for one or more of the following activities in QC including analytical testing in process, stability, and finished products.
In-depth HPLC experience with Empower Software, some protein concentration testing background with strong GMP lab environment experience.
Duties: Testing of in process, stability and finished product samples.
eg HPLC, CE, SDS-PAGE, IEF analytical testing, characterization and sample and data management.
Review and authorisation of Lab Data Support Analytical Technical Transfer activity testing reports and documentation.
Document review/updates when required.
Equipment Calibration, Maintenance and Trouble Shooting.
Method Validation/Verification.
Training of QC Chemistry Laboratory colleagues.
Laboratory Investigation support Laboratory Housekeeping and maintaining GMP standards.
Assisting in regulatory audits.
Education and Experience: Hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology or similar Scientific Subject.
5+ years relevant experience in a pharmaceutical/healthcare environment.
Have strong technical writing skills.
Be detail oriented, self-motivated with good troubleshooting and problem solving abilities.
Experience with analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing would also be advantageous.
If interested in this posting please feel free to contact Avishek Singh at Avishek.sing or for further information.
This advertiser has chosen not to accept applicants from your region.
8
Quality Control Inspector 1 (Evening Shift)
Limerick, Munster
Cook Medical
Posted today
Job Viewed
Job Description
Overview The primary function of this role is the inspection of raw materials (IQC), finished devices (FQC), packaged devices (PKQC) , sterilised devices (PSQC) and device history records (Batch Release) ensuring that inspection procedures are followed at all times and that all product and paperwork passes specified quality control requirements before shipping to customers. Reporting to: Supervisor, Quality Control Find out more about Cook Medical here Responsibilities Ensure that all products which are manufactured at Cook Medical are inspected as per the relevant FQC instructions and that it meets the required quality control specifications before it is shipped to customers. Ensure that all raw materials received on site at Cook Medical are inspected as per the relevant IQC instructions and that they meet the required quality control specifications before release for use in manufacturing. Ensure that finished goods packaged at Cook Medical are inspected as per the relevant packaging quality control instructions and that they meet the required quality control specifications. Ensure that product which has completed the sterilisation cycle is inspected as per the relevant instructions and that its meets the quality control specifications before it is shipped to customers. Ensure that all device history records are reviewed in line with Batch Release procedures and are compliant before product is released to stock. Ensure compliance with GMP practices i.e. gowning correctly, adhering to CMA rules, adhering to relevant line clearance procedures, following procedures and completion of paperwork accurately. Highlight any potential issues to Team Leaders. Contribute to attainment of overall KPI targets for the QC group by achieving daily/weekly quality and output targets. Working as part of a QC team within the Controlled Manufacturing Areas. Ensure that Cook's Code of conduct is considered in all business matters carried out on Cook's behalf. Qualifications Experience in a manufacturing environment/QC inspection role. Previous experience in medical devices, while not essential is advantageous. Good communication and inter-personal skills. Ability to work as part of a team. Some flexibility as regards working hours/days. Willingness and availability to travel on company business. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process click the Continue to Application or Login/Register to apply button below.
This advertiser has chosen not to accept applicants from your region.
9