Specialist Quality

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 Qualityto support its development. Would you like to help establish the Quality Systems that will enable reliable and compliant at a new production site?

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

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 powder filling line, 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

In this role, you help build and maintain the Quality System foundation for a new EU/FDA‑compliant manufacturing facility. Throughout construction, commissioning, and the transition to commercial operations, you implement, operationalize, and improve site Quality Systems to ensure full cGMP readiness. This includes translating global standards and regulatory requirements into practical, site‑specific processes that enable safe and compliant manufacturing. As a subject matter expert, you provide system oversight, technical guidance and hands‑on support to project teams and site functions. You ensure systems are robust, inspection‑ready, and aligned with the 7 attributes of a strong QMS, while also contributing to global harmonization through cross‑site collaboration. Success requires a proactive, analytical, and solution‑oriented mindset. You balance regulatory expectations with practical implementation, support audits and regulatory inspections, promote continuous improvement and Lean behaviors, and coach colleagues to strengthen quality culture. Your work ensures a future‑proof QMS and prepares the facility to deliver safe, high‑quality products at start‑up and beyond.

Key tasks and responsibilities

• Own and continuously improve assigned Quality Systems to ensure cGMP‑compliant, robust performance.
• Translate GMP requirements into practical site procedures and tools to support readiness.
• Oversee Investigations & CAPA, ensuring timely and compliant closure.
• Provide system and compliance expertise for investment projects and validated status.
• Review qualification documentation for equipment, software, and facilities.
• Lead internal audits for assigned systems and monitor CAPA progress.
• Support supplier management activities, including audits and TQAs.
• Prepare for and support regulatory inspections and implement system updates.
• Maintain key site quality documents (e.g., SMF, VMP, CCS, Compliance Plan).
• Lead change management and documentation processes for assigned systems.
• Act as point of contact for inter‑site quality agreements and coordination.
• Promote safety and help integrate QMS, Lean, and continuous improvement behaviors.
• Coach colleagues and contribute to quality strategy through system performance insights.

Your profile

• Degree-qualified in a relevant scientific discipline (BSc or MSc in Pharmacy, Medical Biology, Chemistry, Process Technology or similar)
• A minimum of 10 years’ broad Quality (Systems) experience, EU and FDA, in an international pharmaceutical/animal‑health environment, preferably experience within a production facility.
• Detail‑oriented and risk‑aware, with strong systems thinking to translate global GMP requirements into practical site solutions and the drive to deliver project milestones on schedule.
• Excellent communicator who can engage diverse stakeholders, coach and develop colleagues, and champion continuous improvement and Lean practices while always prioritizing safety, product quality and regulatory compliance.
• 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: 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, Accountability, Adaptability, Aseptic Manufacturing, Audit Management, cGMP Compliance, Contamination Control, Data Analysis, Decision Making, Documentation Review, Documentations, FDA Regulations, GMP Compliance, Interpersonal Relationships, IS Audit, Laboratory Operations, Laboratory Quality Control, Pharmaceutical Management, Project Management, Quality Inspections, Quality Management, Quality Operations, Quality Standards, Regulatory Compliance, Regulatory Inspections {+ 4 more}

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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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

*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.

Requisition ID: R385097