Quality Control Support Specialist
MSD UK
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Benefits offered by this job
Job summary
MSD UK is seeking a Quality Control Support Specialist to help build a new QC organization in Boxmeer. You will act as a senior technical expert, ensuring GMP compliance, driving improvements, and supporting operational excellence within the new facility.
The role collaborates across functions to strengthen quality systems, support inspection readiness, and contribute to establishing and growing the Boxmeer West site. A strong background in GMP and QC is required.
Qualifications
- Bachelor’s degree in Life Sciences or related field.
- Minimum 4–6 years in a GMP-regulated pharmaceutical or life sciences environment.
- Experience leading cross-functional projects and continuous improvement initiatives.
- Strong knowledge of GMP regulations, quality systems, investigations, CAPA and change control.
Responsibilities
- Act as the QC SME for GMP compliance, quality systems, stability studies, LIMS implementation, and equipment lifecycle management.
- Lead investigations, deviations, root cause analyses, and CAPA activities.
- Own and drive quality system processes including change control, investigations, CAPA, and compliance initiatives.
- Review and approve GMP documentation (SOPs, protocols, validation documents, reports).
- Ensure lab operations comply with site procedures, global standards, regulatory requirements, and inspection readiness.
- Lead qualification, validation, calibration, and implementation of lab equipment and new tech.
- Drive continuous improvement, digitalization, automation, and efficiency across QC and cross-functional teams.
- Provide expert support to lab operations, QA, Manufacturing, and stakeholders on quality matters.
- Monitor data, trends, and performance metrics; translate insights into action.
- Lead cross-functional projects, mentor colleagues, deliver GMP training, and represent QC during audits.
Skills
Education
Tools
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.
- 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.
- 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.
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.
Required Skills:Continuous Improvement, Good Laboratory Practices (GLPs), Manufacturing, Pharmaceutical Industry, QC Microbiology, Quality Management Systems (QMS), Teamwork
Continuous Improvement, Good Laboratory Practices (GLPs), Manufacturing, Pharmaceutical Industry, QC Microbiology, Quality Management Systems (QMS), Teamwork
Regular
Not Applicable
09/14/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
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