204 Supplier Quality Engineer jobs in Ireland

Within this role you will be responsible for the oversight of Quality Control support operations. As a Manager within Quality Control a typical day might include, but is not limited to, the following: Maintaining oversight of QC equipment lifecycle activities (including procurement, installation, qualification, maintenance, and decommissioning) Providing direction to Managers and staff that support the equipment Ensuring equipment qualification and maintenance programs are aligned with regulatory agencies requirements, qualified and available for QC laboratory usage Interacting with QC partner groups to establish internal requirements for equipment Leading QC equipment validation / qualification efforts through partnering and interaction with QA Validation and IT groups Managing oversight of the preventive and corrective maintenance monitoring program Managing oversight of the QC external laboratories activities and performance monitoring of external testing laboratories Supervising the issuance and approval of Quality agreements and SLAs with the contract labs Verifying that the site Manufacturing licence and global procedures reflect current contract lab utilization Identifying and calling out issues at contract laboratories to QC leadership Sourcing, co-ordinating and project management of GMP activities relating to new contract lab introduction Travel may be required in support of external contract laboratory testing activities Performing personnel management functions including time sheet submissions, scheduling of vacations, personnel development, and performance evaluations Responsibility for equipment automation and associated projects This role might be for you if you: Possess strong communication and interpersonal skills Demonstrate logical troubleshooting and problem-solving skills Have a detailed understanding of equipment qualification and maintenance activities and industry compliance norms Have the ability to communicate effectively with multiple partners Enjoy working in a fast-paced environment Demonstrate a collaborative and team-orientated approach To be considered for this opportunity you should have a BA/BS in chemistry, biology or related field with 8+ years' proven experience preferably in the pharmaceutical or biotechnology industry, and previous supervisory or leadership experience. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels! Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U. positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location. Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Excel Recruitment is seeking a Quality Control Officer for our client who specialises in the fresh produce and food distribution industry.

This is an exciting opportunity to join a company with a proud heritage and a strong commitment to quality, innovation, and customer service.

Job description Key Responsibilities and Duties Approve incoming materials by confirming specifications, conducting a visual and measurement test, and rejecting and returning unacceptable materials.

Approve all finished products by confirming specifications and conducting required tests.

Completion of daily records/ traceabilities Ensuring food safety is maintained throughout the process in accordance with BRC and Bord Bia standards.

A lot of walking / standing / checking of products in different areas of the packhouse such as Goods-In, Packhouse & Goods-Out Qualifications/Experience Level 7 in food science or similar qualification.

Experience in a quality role is desired but not essential.

Key Behaviours Excellent attention to detail Excellent communication skills Ability to work on own initiative If you or anyone you know would be interested in this role, please apply with your CV or contact Ciaran #INDUST Skills: quality control officer quality control officer

Within this role you will be responsible for the oversight of Quality Control support operations.

As a Manager within Quality Control a typical day might include, but is not limited to, the following: Maintaining oversight of QC equipment lifecycle activities (including procurement, installation, qualification, maintenance, and decommissioning) Providing direction to Managers and staff that support the equipment Ensuring equipment qualification and maintenance programs are aligned with regulatory agencies requirements, qualified and available for QC laboratory usage Interacting with QC partner groups to establish internal requirements for equipment Leading QC equipment validation / qualification efforts through partnering and interaction with QA Validation and IT groups Managing oversight of the preventive and corrective maintenance monitoring program Managing oversight of the QC external laboratories activities and performance monitoring of external testing laboratories Supervising the issuance and approval of Quality agreements and SLAs with the contract labs Verifying that the site Manufacturing licence and global procedures reflect current contract lab utilization Identifying and calling out issues at contract laboratories to QC leadership Sourcing, co-ordinating and project management of GMP activities relating to new contract lab introduction Travel may be required in support of external contract laboratory testing activities Performing personnel management functions including time sheet submissions, scheduling of vacations, personnel development, and performance evaluations Responsibility for equipment automation and associated projects This role might be for you if you: Possess strong communication and interpersonal skills Demonstrate logical troubleshooting and problem-solving skills Have a detailed understanding of equipment qualification and maintenance activities and industry compliance norms Have the ability to communicate effectively with multiple partners Enjoy working in a fast-paced environment Demonstrate a collaborative and team-orientated approach To be considered for this opportunity you should have a BA/BS in chemistry, biology or related field with 8+ years' proven experience preferably in the pharmaceutical or biotechnology industry, and previous supervisory or leadership experience.

#JOBSIEPR Does this sound like you? Apply now to take your first step towards living the Regeneron Way.

We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations.

The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.

S., the salary ranges provided are shown in accordance with U.

S.

law and apply to U.

positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency.

If you are outside the U.

S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process.

Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted.

The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Excel Recruitment is seeking a Quality Control Officer for our client who specialises in the fresh produce and food distribution industry. This is an exciting opportunity to join a company with a proud heritage and a strong commitment to quality, innovation, and customer service. Job description Key Responsibilities and Duties Approve incoming materials by confirming specifications, conducting a visual and measurement test, and rejecting and returning unacceptable materials. Approve all finished products by confirming specifications and conducting required tests. Completion of daily records/ traceabilities Ensuring food safety is maintained throughout the process in accordance with BRC and Bord Bia standards. A lot of walking / standing / checking of products in different areas of the packhouse such as Goods-In, Packhouse & Goods-Out Qualifications/Experience Level 7 in food science or similar qualification. Experience in a quality role is desired but not essential. Key Behaviours Excellent attention to detail Excellent communication skills Ability to work on own initiative If you or anyone you know would be interested in this role, please apply with your CV or contact Ciaran #INDUST Skills: quality control officer quality control officer

Within this role you will be responsible for the oversight of Quality Control support operations.

As a Manager within Quality Control a typical day might include, but is not limited to, the following: Maintaining oversight of QC equipment lifecycle activities (including procurement, installation, qualification, maintenance, and decommissioning) Providing direction to Managers and staff that support the equipment Ensuring equipment qualification and maintenance programs are aligned with regulatory agencies requirements, qualified and available for QC laboratory usage Interacting with QC partner groups to establish internal requirements for equipment Leading QC equipment validation / qualification efforts through partnering and interaction with QA Validation and IT groups Managing oversight of the preventive and corrective maintenance monitoring program Managing oversight of the QC external laboratories activities and performance monitoring of external testing laboratories Supervising the issuance and approval of Quality agreements and SLAs with the contract labs Verifying that the site Manufacturing licence and global procedures reflect current contract lab utilization Identifying and calling out issues at contract laboratories to QC leadership Sourcing, co-ordinating and project management of GMP activities relating to new contract lab introduction Travel may be required in support of external contract laboratory testing activities Performing personnel management functions including time sheet submissions, scheduling of vacations, personnel development, and performance evaluations Responsibility for equipment automation and associated projects This role might be for you if you: Possess strong communication and interpersonal skills Demonstrate logical troubleshooting and problem-solving skills Have a detailed understanding of equipment qualification and maintenance activities and industry compliance norms Have the ability to communicate effectively with multiple partners Enjoy working in a fast-paced environment Demonstrate a collaborative and team-orientated approach To be considered for this opportunity you should have a BA/BS in chemistry, biology or related field with 8+ years' proven experience preferably in the pharmaceutical or biotechnology industry, and previous supervisory or leadership experience.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels! Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations.

The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.

S., the salary ranges provided are shown in accordance with U.

S.

law and apply to U.

positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency.

If you are outside the U.

S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process.

Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted.

The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Junior to Mid-Level Quality Control/Validation Engineer IRELAND, IRELAND / NORTH EUROPE / FULL TIME About CAI: CAI is a 100% employee-owned company established in 1996, growing year over year to nearly 700 employees worldwide. We provide commissioning, qualification, validation, start-up, project management, and consulting services related to operational readiness in FDA regulated and other mission-critical industries. Are You Ready?: Our approach is simple: we put the clients interests first, we do not stop until it is right, and we will do whatever it takes to get there. As owners of CAI, we are committed to living our Foundational Principles, both professionally and personally: - We act with integrity - We serve each other - We serve society - We work for our future With employee ownership, one persons success is everyones success. We work diligently to accomplish team goals. We place Team Before Self, demonstrate Respect for Others, and possess a can-do attitude. That is how we have grown exponentially. CAI agents will be exposed to cutting-edge technologies in the advanced medicine space, working alongside recognized subject matter experts. As part of our culture, we invest in YOUR future through hands-on certifications and professional training. Position Overview: We are looking for a Junior to Mid-Level Validation Engineer to join our growing operations in Ireland. This role is designed for individuals with at least 2 years of relevant experience in Validation Engineering or Quality Control. As a Junior to Mid-Level Engineer, you will work alongside senior team members, assisting in maintaining quality standards and ensuring compliance throughout all equipment qualification activities. Key Responsibilities: - Support and assist with Quality Control compliance for equipment qualification activities, ensuring adherence to safety and regulatory standards. - Help document and execute equipment qualification processes, from initial assessments to Operational Qualification (OQ), focusing on accuracy and attention to detail. - Follow established procedures and protocols for new equipment qualification to help embed quality practices within workflows. - Assist with the review and completion of Test Outlines and Procedures (TOPs), verifying alignment with quality specifications. - Support the planning and organization of commissioning materials and consumables, ensuring they meet required quality standards. - Monitor equipment qualification activities to ensure that timelines are met while maintaining high quality standards. - Assist in preparing and maintaining Qualification Summary Reports (QSRs) and related documentation to ensure compliance with quality standards. - Participate in equipment Design Evaluations, Factory Acceptance Testing (FAT), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), with a focus on achieving quality outcomes. - Assist in managing quality control processes related to equipment qualifications, including documentation control, change controls, and punch list tracking. - Collaborate with project contractors and equipment vendors to perform and verify tests, ensuring quality control is upheld. - Provide support for quality assurance tasks throughout the equipment qualification process, ensuring consistent quality standards are maintained. Position Requirements: - BS or MS in a relevant science or engineering field, or equivalent experience. - 2+ years of industry-related experience in a similar role. - Strong oral and written communication skills, with a focus on clear documentation and reporting. - Strong problem-solving skills with a focus on Quality Control. - Customer-service oriented and able to collaborate well with internal teams and external vendors. - Familiarity with life science manufacturing processes such as biotech, aseptic fill/finish, oral solid dose (OSD), and gene therapy, or equivalent experience. - Willing and able to travel domestically and internationally, if required. Skills: Quality Control QC Technican Equipment Validation Life Science Bio-Pharma Pharmaceutical Manufacturing Benefits: Pension Fund Medical Aid / Health Care Dental Care Income Protection Group Life Assurance

Junior to Mid-Level Quality Control/Validation Engineer IRELAND, IRELAND / NORTH EUROPE / FULL TIME About CAI: CAI is a 100% employee-owned company established in 1996, growing year over year to nearly 700 employees worldwide.

We provide commissioning, qualification, validation, start-up, project management, and consulting services related to operational readiness in FDA regulated and other mission-critical industries.

Are You Ready?: Our approach is simple: we put the clients interests first, we do not stop until it is right, and we will do whatever it takes to get there.

As owners of CAI, we are committed to living our Foundational Principles, both professionally and personally: - We act with integrity - We serve each other - We serve society - We work for our future With employee ownership, one persons success is everyones success.

We work diligently to accomplish team goals.

We place Team Before Self, demonstrate Respect for Others, and possess a can-do attitude.

That is how we have grown exponentially.

CAI agents will be exposed to cutting-edge technologies in the advanced medicine space, working alongside recognized subject matter experts.

As part of our culture, we invest in YOUR future through hands-on certifications and professional training.

Position Overview: We are looking for a Junior to Mid-Level Validation Engineer to join our growing operations in Ireland.

This role is designed for individuals with at least 2 years of relevant experience in Validation Engineering or Quality Control.

As a Junior to Mid-Level Engineer, you will work alongside senior team members, assisting in maintaining quality standards and ensuring compliance throughout all equipment qualification activities.

Key Responsibilities: - Support and assist with Quality Control compliance for equipment qualification activities, ensuring adherence to safety and regulatory standards.

- Help document and execute equipment qualification processes, from initial assessments to Operational Qualification (OQ), focusing on accuracy and attention to detail.

- Follow established procedures and protocols for new equipment qualification to help embed quality practices within workflows.

- Assist with the review and completion of Test Outlines and Procedures (TOPs), verifying alignment with quality specifications.

- Support the planning and organization of commissioning materials and consumables, ensuring they meet required quality standards.

- Monitor equipment qualification activities to ensure that timelines are met while maintaining high quality standards.

- Assist in preparing and maintaining Qualification Summary Reports (QSRs) and related documentation to ensure compliance with quality standards.

- Participate in equipment Design Evaluations, Factory Acceptance Testing (FAT), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), with a focus on achieving quality outcomes.

- Assist in managing quality control processes related to equipment qualifications, including documentation control, change controls, and punch list tracking.

- Collaborate with project contractors and equipment vendors to perform and verify tests, ensuring quality control is upheld.

- Provide support for quality assurance tasks throughout the equipment qualification process, ensuring consistent quality standards are maintained.

Position Requirements: - BS or MS in a relevant science or engineering field, or equivalent experience.

- 2+ years of industry-related experience in a similar role.

- Strong oral and written communication skills, with a focus on clear documentation and reporting.

- Strong problem-solving skills with a focus on Quality Control.

- Customer-service oriented and able to collaborate well with internal teams and external vendors.

- Familiarity with life science manufacturing processes such as biotech, aseptic fill/finish, oral solid dose (OSD), and gene therapy, or equivalent experience.

- Willing and able to travel domestically and internationally, if required.

Skills: Quality Control QC Technican Equipment Validation Life Science Bio-Pharma Pharmaceutical Manufacturing Benefits: Pension Fund Medical Aid / Health Care Dental Care Income Protection Group Life Assurance

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.
We're excited to invite you to lead our Quality Control (QC) Chemistry Laboratory team in our purification and aseptic filling facility at Grifols Worldwide Operations (GWWO). As **QC Chemistry Manager** , you will play a key role in ensuring high-quality laboratory testing of clean utility, raw material, in-process and final container materials, maintaining full compliance with current Good Manufacturing Practices (cGMP) and safety standards.
**Key Responsibilities:**
- Management of the QC Chemistry team to carry out required chemistry, immunochemistry and protein testing as required
- Ensure QC testing of clean utility, raw material, in-process and final container testing is performed as per the production plan
- Manage integrity of Laboratory Data
- Ensure all methods are qualified/validated in line with site procedures and regulatory/compendial requirements
- Ensure all equipment is validated, maintained, calibrated, and requalified in line with site procedures and regulatory/compendial requirements
- Creation, review and update of test methods and SOPs to ensure all aspects of compliance are adhered to
- Drive and oversee process/product/OOS/deviation investigations
- Implementation of Corrective and Preventative Actions
- Maintain, monitor and report QC Chemistry metrics and KPIs
- Ensure training and development of QC Chemistry team members in conjunction with team development and goals via the performance management process
- Represent QC Chemistry in any regulatory, corporate or internal audits
- Ensure regular Quality interaction with other departments within GWWO and Grifols sister sites
- Support site quality activities, including but not limited to: Annual Product Quality Reviews (APQRs), recall activities, change control etc.
- Responsible for any projects impacting QC Chemistry such as Method Transfers, Process Improvement or Harmonisation Projects
- Keep Abreast of the latest developments from regulatory authorities in relation to Quality Compliance activities
- Manage the safety and performance of QC Chemistry in line with safety regulations and site procedures
- Perform additional duties as assigned
- Act as a delegate for activities performed by the QC Senior Manager for QC Chemistry activities
**Knowledge & Skills:**
- Full understanding of relevant cGMP, quality and compliance regulations
- Experience with chromatography instrumentation and methods
- Experience with protein chemistry instrumentation and methods
- Method Transfer and qualification experience
- Understanding of pharmacopoeial requirements and methods
- Excellent communication skills at organisation, team and individual levels
- Demonstrated problem solving skills
- Strong decision making skills
- Strong presentation skills
- Ability to manage multiple projects to plan/budget
- Experience in developing analytical methods is desirable
- Experience with Statistical Process Control (SPC) is desirable
- Experience with Lab Management Systems & SAP is desirable
**Qualifications:**
- BSc or equivalent in chemistry, biochemistry, pharmaceutical science or related field
- Minimum 3 years supervisory/management experience
- 8 years progressive experience as an individual contributor in a fast paced GMP Laboratory environment
- M.Sc. qualification is desirable but not essential
**Our Benefits Include:**
+ Highly competitive salary
+ Group pension scheme - Contribution rates up to 7%
+ Private Medical Insurance for the employee
+ Ongoing opportunities for career development in a rapidly expanding work environment
+ Succession planning and internal promotions
+ Education allowance
+ Wellness activities - Social activities eg. Golf, Padel, Summer Events
We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply - we're excited to hear from you.
#LI-FD1
**Location: Grange Castle International Business Park, Grange, Co. Dublin, D22 K2R3 ( more about Grifols
**Req ID:**
**Type:** Regular Full-Time
**Job Category:**

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.