Quality Control Support Specialist
Quick Summary
Job Description This is a unique opportunity to help build a new Quality Control organization from the ground up, combining technical expertise, innovation,
Job Description
This is a unique opportunity to help build a new Quality Control organization from the ground up, combining technical expertise, innovation, and leadership to support the future of animal health manufacturing in Boxmeer. Join us as a:
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.
The Quality Control Support Specialist is a senior technical expert within the Quality Control organization, playing a key role in ensuring GMP compliance, driving continuous improvement, and supporting operational excellence. Acting as a trusted Subject Matter Expert, you will collaborate across functions to strengthen quality systems, support inspection readiness, and contribute to the successful establishment and growth of the new Boxmeer West manufacturing facility.
Responsibilities
~1 min read- →Act as the Quality Control Subject Matter Expert (SME) for GMP compliance, quality systems, stability studies, LIMS implementation, and laboratory equipment lifecycle management.
- →Lead complex investigations, deviations, root cause analyses, and CAPA activities, ensuring timely and effective resolution.
- →Own and drive quality system processes, including change controls, investigations, CAPAs, and compliance-related initiatives.
- →Review and approve GMP documentation, including SOPs, protocols, validation documents, technical reports, and work instructions.
- →Ensure laboratory operations comply with site procedures, global standards, and regulatory requirements, maintaining inspection readiness at all times.
- →Lead and support qualification, validation, calibration, and implementation activities for laboratory equipment, systems, and new technologies.
- →Drive continuous improvement, digitalization, automation, and efficiency projects across Quality Control and cross-functional teams.
- →Provide expert support to laboratory operations, Quality Assurance, Manufacturing, and other stakeholders on quality and compliance matters.
- →Monitor laboratory data, trends, and performance metrics, translating insights into actions that enhance quality, compliance, and operational excellence.
- →Lead cross-functional projects, mentor colleagues, deliver GMP training, and represent Quality Control during audits, inspections, and management reviews.
- Bachelor’s degree in Life Sciences, Chemistry, Microbiology, Biotechnology, Pharmaceutical Sciences or a related field.
- At least 4-6 years experience in a GMP-regulated pharmaceutical, biotechnology or life sciences environment.
- Proven track record of leading cross-functional projects and driving continuous improvement initiatives.
- Strong knowledge of GMP regulations, quality systems, investigations, CAPA management, change control, qualification and validation processes.
- Solid understanding of Quality Control laboratory operations, analytical methods and regulatory expectations.
- Experience working with LIMS, SAP, computerized laboratory systems and digital quality management platforms.
- Strong analytical and problem-solving skills, with experience in data analysis, trending and performance monitoring.
- Excellent project management, stakeholder management and influencing skills, with the ability to drive change across functions.
- Demonstrated leadership, coaching and mentoring capabilities, combined with strong technical writing and presentation skills.
- Excellent verbal and written communication skills in Dutch and English.
What We Offer
~1 min readThe 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.
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.
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.
Requirements
~1 min readLocation & Eligibility
Listing Details
- Posted
- September 24, 2026
- First seen
- October 1, 2026
- Last seen
- October 1, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 28%
- Scored at
- October 1, 2026
Signal breakdown
Stay ahead of the market
Get the latest job openings, salary trends, and hiring insights delivered to your inbox every week.
No spam. Unsubscribe at any time.