Associate Specialist Quality Control Support

Job Description

We are looking for a new colleague who brings energy, accuracy, and a strong quality mindset. You will help ensure smooth laboratory operations and support our commitment to high-quality, compliant processes. Are you ready to make an impact in our Animal Health organization?

For our Animal Health location in Boxmeer, we are currently recruiting an Associate Specialist Quality Control Support.

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).

Purpose of the role

The purpose of this role is to act as the deputy Lab Manager and ensure the smooth execution of daily Quality Control laboratory operations. This includes planning, reviewing, writing and approving protocols, as well as acting as subject matter expert with respect to Quality Control deviations, CAPAs, and GMP-related changes, and providing GMP support to the Quality Control organization by coordinating compliance-driven projects. The role promotes strong collaboration across teams, leads and participates in TIER meetings, and serves as a Subject Matter Expert (SME) during site audits, regulatory inspections, and corporate reviews. Additionally, the position contributes to cross-functional and global initiatives, supports laboratory investigations through impact assessments and root cause analysis, and upholds the highest standards of integrity, safety, quality, and environmental responsibility. The role requires strong communication skills, a proactive and flexible mindset, customer focus, computer literacy, and a team-oriented approach to ensure the continued reliability and compliance of laboratory operations.

Tasks and responsibilities

Act as subject matter expert for the QC support tasks and oversee daily operations.

• Supports SAP/LIMS implementation, updates, and ongoing maintenance.
• Oversees equipment maintenance, calibration, and qualification activities.
• Performs QC investigations, including impact assessments (product, process, validation, etc.), Root Cause Analysis (RCA), and preparation of investigation protocols and deviation reports.
• Manages QC changes (e.g., analytical procedures), including writing and updating documents and associated analysis data sheets / CJA’s according to applicable guidelines.
• Coordinates and administers documentation related to deviations, CAPAs, and QC projects in compliance with site SOPs, company guidelines/procedures, and regulatory requirements.
• Orders laboratory supplies and ensures timely availability of materials.
• Guides QC personnel on quality-related matters and ensures implementation of quality improvements, procedures, and best practices.

Your profile

• A Bachelor’s degree (HBO or HLO), preferably in a scientific field, or equivalent relevant work experience.
• More than 3 years of relevant experience in Quality Control within the pharmaceutical industry.
• Yellow / Green Belt certified and applies continuous improvement methodologies.
• Solid knowledge of and experience with quality and compliance guidelines, including cGMP.
• Familiarity with industry guidance and regulations related to Stability program, Equipment Qualification, Quality Control, Quality (Management) Systems, Documentation, QC Deviations/CAPA, and Change Controls.
• Strong technical knowledge of testing techniques.
• Experience with Technical Writing, Root Cause Analysis, Failure Mode & Effect Analysis (FMEA), CAPA development, and Lean Six Sigma.
• Effective project management and planning skills, with the ability to communicate priorities clearly and align stakeholders.
• Ability to translate a quality-focused mindset into daily practice and bring others along.
• Excellent interpersonal and written/verbal communication skills in both Dutch and English.
• Experience with documentation system 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.

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:

Accountability, Customer Experience Management, Data Analysis, GMP Compliance, Good Laboratory Practices (GLPs), Keen Observation, QC Microbiology, Quality Control Management, Quality Management, Root Cause Analysis (RCA), Team Orientation, Technical Procedures