Job Description:

Are you looking for a highly independent, hands‑on project role with both operational and strategic responsibilities? At our Animal Health site in Boxmeer, we are building a new manufacturing facility and are seeking a Specialist Quality to support its development. Would you like to help establish the Quality Systems that will enable reliable and compliant operations at a new production site?

For our Animal Health location Boxmeer, we are currently recruiting an Associate Specialist Quality Control 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. To accelerate delivery of robust, compliant, and future‑proof Quality Systems that will enable safe and compliant product manufacture, we are looking for a Specialist Quality.

Purpose of the role

The purpose of this role is to support and deputize for the Lab Manager by ensuring smooth and compliant daily quality control laboratory operations. This includes oversight of planning, execution, review, and approval of test results, as well as acting as subject matter expert with respect to QC deviations, CAPAs, and GMP‑related changes. The role provides essential GMP support to the QC organization by coordinating and driving compliance‑focused projects that maintain the integrity of laboratory processes.

Beyond operational responsibilities, the role ensures high‑quality execution of quality control activities through strong project management, clear prioritization, and effective communication to align and guide stakeholders. It translates a quality‑driven mindset into practical daily practices and supports others in adopting these standards. Success in this role requires solid digital literacy, a strong client‑ and end‑user‑focused approach, proactive and flexible communication, and a collaborative, team‑oriented attitude. Demonstrating a flawless integrity mindset in all decisions and actions is fundamental to ensuring consistent compliance and operational excellence.

Tasks and responsibilities

• Act as subject matter expert for the QC chemistry laboratory and manage daily operations.
• Perform QC investigations, including impact assessments (product, process, validation), Root Cause Analysis (RCA), and preparation of investigation protocols and deviation reports.
• Manage QC chemistry‑related changes (e.g., analytical procedures), including writing and updating documents and associated analysis data sheets/CJAs.
• Coordinate and administer documentation related to deviations, CAPAs, and QC projects in compliance with site SOPs, company guidelines/procedures, and regulatory requirements.
• Participate in site audits, regulatory inspections, and corporate audits, including providing SME support for audit responses.
• Attend and lead TIER meetings.
• Conduct and support stability studies.
• Always adhere to GxP and safety guidelines. Write, review, and modify technical reports, instructions, and procedures within relevant discipline(s).
• Guide QC personnel on quality issues and ensure implementation of quality improvements, procedures, and guidelines.
• Participate in cross‑functional and global teams.
• Actively contribute to corporate safety, health, and environmental policies, demonstrating personal commitment to safe, healthy, and environmentally responsible working practices.

Your profile

• Bachelor degree (HBO or HLO) in (Bio)Chemistry, Analytical Science, or a related scientific field, or comparable work experience.
• More than 3 years of relevant Quality Control experience in the pharmaceutical industry.
• Knowledge and experience with quality and compliance guidelines, cGMPs (EU and preferably US FDA).
• Knowledge of industry guidance and regulations for Analytical Methods Validation, Equipment Qualification, Quality Control, Quality (Management) Systems, Documentation, QC Deviations/CAPA, and Change Controls.
• Technical knowledge of analytical testing techniques (UV, UPLC/HPLC, GC, particle distribution, dissolution).
• Experience with Technical Writing, Root Cause Analysis, FMEA, CAPA establishment, and Lean Six Sigma.
• Effective project management and prioritization skills with strong communication abilities.
• Excellent interpersonal and communication skills in Dutch and English.
• Experience with documentation systems and preferably with LIMS.

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.

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.

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.

Required Skills:

Accountability, Aseptic Manufacturing, Data Analysis, Documentations, Good Laboratory Practices (GLPs), Keen Observation, Laboratory Instrumentation, Technical Procedures, Technical Writing

Preferred Skills:

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Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

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Hazardous Material(s):

Job Posting End Date:

03/27/2026

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