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

For our Animal Health location in 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.
• 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.
• 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.

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.

Required Skills

Adaptability, cGMP Compliance, Project Management, Quality Inspections, Quality Management, Quality Operations, Quality Standards, Regulatory Compliance, Supplier Relationship Management