Senior Lab Technician Chemistry

Job Description

Do you want to play a critical role in maintaining GMP compliance, driving quality improvements and supporting the successful start-up and operation of our new manufacturing facility in Boxmeer. For our growing Quality Control organization, we are looking for a:

Senior Lab Technician Chemistry

Welcome to our team

Our production facilities in Boxmeer are part of our global Animal Health production network and manufacture and package animal health products according to Good Manufacturing Practice standards (GMP). Currently, we are investing in a new EU and FDA compliant manufacturing facility, which includes a Quality Control laboratory, in Boxmeer to bring our latest animal health innovations to market. Once the manufacturing facility is fully operational (expected in 2030), it will create about 80–100 FTE jobs. The facility will include dedicated warehouse, manufacturing, quality assurance, quality control, and packaging & labeling teams to deliver high quality, compliant products.

Purpose of the role

As a Senior Lab Technician Chemistry you will support the Lab Manager by ensuring efficient, compliant, and high-quality Quality Control laboratory operations. You will perform initially method transfer activities to later support QC testing such as stability, release, IPC. You will also be involved in investigations, deviations, CAPAs, change controls and GMP compliance activities. The position promotes a strong quality culture by guiding QC personnel, driving process improvements and translating compliance requirements into effective day-to-day practices.

Tasks and responsibilities include but are not limited to

• Support QC laboratories and external groups as Subject Matter Expert (SME) for specific analytical techniques.
• Execute, review and report routine and non-routine analytical tests and laboratory activities according to approved procedures and guidelines.
• Perform first-line troubleshooting activities.
• Support QC investigations, including impact assessments, root cause analysis (RCA), deviation management, and investigation reporting.
• Support QC change controls and ensure compliance with GMP requirements, site procedures, and quality standards.
• Write procedures, work instructions, technical reports, and analytical documentation.
• Verify, interpret, and validate complex analytical test results and trends.
• Coordinate maintenance, calibration, qualification, and validation activities to ensure reliable laboratory operations.
• Ensure compliance with cGMP, GxP, regulatory requirements, and internal quality systems.
• Act as SME during audits and inspections, supporting audit readiness and responses.
• Drive continuous improvement initiatives to enhance laboratory processes, quality systems, and operational excellence.

Your profile

• Bachelor's degree (HBO/HLO) in (Bio)Chemistry, Analytical Science,or a related scientific discipline.
• At least 3 years of experience in a Quality Control role within the pharmaceutical, biotechnology or other GMP-regulated environment.
• Strong knowledge of cGMP principles, quality systems, regulatory requirements, deviations, CAPAs, change controls, analytical method validation, and equipment qualification.
• Hands-on experience with analytical testing techniques and laboratory operations.
• Proven experience with technical writing, Root Cause Analysis (RCA), FMEA, CAPA management and continuous improvement methodologies such as Lean Six Sigma.
• A strong quality mindset, with the ability to translate quality and compliance requirements into practical laboratory processes and influence others to do the same.
• Excellent project management, planning, prioritization and problem-solving skills, combined with a structured and proactive approach.
• Strong communication and stakeholder management skills.
• Fluent in Dutch and English, both written and spoken.
• A proactive, flexible, and team-oriented professional with a high level of integrity, accountability, and customer focus.
• Experience working with electronic documentation systems, LIMS, and preferably SAP.

What we offer

The opportunity to step into a new, hands‑on position where you’ll work independently, collaborate across functions and take on real leadership responsibilities. Our benefits are very competitive, and the summary below will give you an idea of what you can expect.

• Competitive salary based on your knowledge and experience.
• 3% year-end payment and an annual bonus based on personal and company performance.
• At least 35.5 days of paid leave.
• Travel allowance and a solid pension scheme.
• A high-quality company restaurant offering fresh and healthy options daily.
• Excellent accessibility: the train station is located directly at our main entrance and there is ample parking available.
• A contribution toward your personal sports membership to support your vitality.
• A beautiful private park on the premises, ideal for a walk, break, or moment of relaxation.
• Mental well-being support through Lyra Health for you and your family members.
• Access to a dedicated prayer and meditation room.
• Extensive development opportunities thanks to the size of the site and the presence of many disciplines and global departments represented in Boxmeer.
• A workplace within an organization that is continuously growing and evolving.

Animal Health

Our Animal Health Division is a trusted global leader in veterinary medicine, dedicated to preserving and improving health, well-being, and performance of animals and the people who care for them. We are a global team of professionals working together to make a positive difference in animal care and the world’s food supply and have a deep sense of responsibility towards our customers, consumers, animals, society, and our planet.

Through our commitment to The Science of Healthier Animals®, we offer veterinarians, farmers, pet owners and governments one of the widest ranges of veterinary pharmaceuticals, vaccines and health management solutions and services as well as an extensive suite of digitally connected identification, traceability and monitoring products. We invest in dynamic and comprehensive R&D resources and a modern, global supply chain. We are present in more than 50 countries, while our products are available in some 150 markets.

For questions about this vacancy

Please send an email including the vacancy number and job title to the following email address: RecruitmentNL@MSD.com. Applications can only be submitted through our career site.

Required Skills:

Chemistry, GMP Laboratory, Laboratory Analytical Techniques, Laboratory Operations, Manufacturing, Product Inspections, Quality Assurance Processes, Standard Operating Procedure (SOP) Writing

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

09/15/2026

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