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 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). Currently, we are investing in a new EU- and FDA-compliant manufacturing facility and Quality Control laboratory 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.

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 the 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 preferable 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, 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

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:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

03/27/2026

*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: R385900