Job Description

Are you looking for a role where you help maintain and improve key Quality Systems within a growing manufacturing environment? At our Animal Health site in Boxmeer, we are hiring an Associate Specialist Quality to support compliant and reliable operations. This role offers the opportunity to play an important part in strengthening the site’s quality foundation.

For our Animal Health location Boxmeer, we are currently recruiting an Associate Specialist Quality

Purpose of the Role

This role is focused on ensuring cGMP compliance for the assigned Quality Systems, to support the implementation, maintenance and operational activities of the Quality Systems for a new manufacturing site. You will play a key part in continuously improving and further developing these systems in alignment with the Site QMS strategy, while also contributing to harmonization across the organization through participation in Global Compliance Work Committees. To be successful in this role, you bring a self‑starting, can‑do attitude, strong analytical and data‑driven thinking, and a solution‑oriented mindset. You are results‑focused, eager to learn, and committed to delivering high‑quality support to your internal customers. Clear communication, strong interpersonal skills, and the ability to balance both people‑ and task‑oriented work complete the profile.

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 and powder filling line in Boxmeer to bring our latest animal health innovations to market. Once the plant is fully operational (expected in 2030), it will create about 80–100 FTE jobs. The facility will include dedicated warehouse, manufacturing, quality, 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 an Associate Specialist Quality.

Key tasks and responsibilities

• Support, maintain, and improve assigned Quality Systems, ensuring robustness, compliance, and alignment with global guidelines, legislation, and cGMP.
• Act as SSO or SSO‑delegate and demonstrate ownership where assigned.
• Monitor and report system performance and drive continuous improvement.
• Apply Quality Systems Thinking and contribute to Permanent Inspection Readiness.
• Support preparation, execution, and follow‑up of inspections.
• Ensure correct application of GMP documentation and support overall site quality oversight.

• Investigations & CAPA: Support compliant processes, maintain oversight, and ensure timely CAPA closure.
• Investment Projects: Act as system expert and support compliant project execution.
• Validated Status: Track validated status and review validation/qualification records.
• Quality Strategy: Translate GMP requirements into local procedures and support system implementation.
• Internal Audits: Execute audits and track CAPA progress.
• Review of qualification documentation of equipment, software and facilities
• Supplier Management: Support audits, TQAs, and supplier assessments.
• Regulatory Inspections: Support preparation, execution, and follow‑up.
• Site Master File & Compliance Plan: Support maintenance and updates.
• Support maintenance of Contamination Control Strategy and Validation Master Plan.
• Change Management & Documentation: Support compliant processes and system oversight.
• Intercompany Complaints & Inter‑Site Relations: Support handling and coordination of agreements.
• Safety Culture: Demonstrate strong safety awareness and adherence to site policies.

What we ask

• Bachelor Degree in a relevant scientific discipline (BSc in Chemistry, Process Technology or similar).
• Experienced in GMP/Quality related role (3 – 5 Years), experienced in GxP (preferably EU and FDA), preferably experience in a quality control environment.
• Knowledge of internal and external compliance requirements and quality guidelines;
• Project management understanding and capable to fulfill project team roll
• Developing auditing skills.
• Fluent in English and Dutch (or willing and able to learn Dutch quickly).
• Based within a reasonable commuting distance of Boxmeer and available onsite at least four days per week.

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: [email protected]

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:

Analytical Problem Solving, Analytical Problem Solving, Aseptic Filling, cGMP Compliance, Change Management, Communication, Complaint Management, Contamination Control, Continuous Process Improvement, Decision Making, Deviation Management, Good Manufacturing Practices (GMP), Internal Auditing, Quality Assurance (QA), Quality Auditing, Quality Management, Quality Management Standards, Quality Management Systems (QMS), Quality Standards, Quality Support, Root Cause Analysis (RCA), Safety Awareness, Safety Culture, Supplier Management, Supplier Relationship Management {+ 5 more}

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:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

03/24/2026

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