International Seed Management Specialist

Job Description

Help ensure safe, compliant seed management for Animal Health vaccines, your expertise will make a global impact from day one.

For our team located in Boxmeer we are looking for an:

International Seed Management Specialist

Welcome in our team

The International Seed Management (ISM) group is part of Bioprocess Technology Solutions. ISM manages the global production, testing, documentation, and storage of master, working, and first-production seeds, as well as production cells, supporting continuous manufacturing and timely registration of Animal Health vaccines and biologics.

Bioprocess Technology Solutions partners closely with R&D and Manufacturing to ensure robust product introductions, smooth transfers, and reliable supply. The team brings deep expertise in viral cell culture, bacterial fermentation, downstream processing, purification, freeze-drying, and vaccine formulation.

About the role

As an International Seed Management Specialist, you will lead risk assessments for extraneous agents testing, oversee seed production and quality control activities and partner with R&D and Manufacturing to maintain high-quality, compliant seeds that support continuous supply. You will also help refine procedures, align with regulatory expectations and contribute to global seed management policies and guidance.

Tasks and responsibilities include but are not limited to  

• Act as the seed Subject Matter Expert for the EU/global region (ex-US), guiding compliant production and Quality Control.
• Partner with global teams on seed production, testing and compliance.
• Lead Master Seed testing and specifications, advising on materials, volumes, containers, labeling, storage and test plans.
• Authorize and release Master, Working, and first Production Seed batches; maintain lineage records and coordinate shipments.
• Prepare QC test summaries for registration dossiers and verify compliance of seed dossier sections.
• Shape and maintain global seed management policies; track regulatory changes and drive implementation with R&D and Manufacturing.
• Represent ISM on transfer teams; advise on resources, risks and timelines; support audits and policy adherence checks.
• Champion continuous improvement across seed management, GLP/GMP, Health & Safety and IT; coach and mentor colleagues.
• Co-lead and contribute to inclusive, cross-functional projects with global stakeholders.

Your profile

• Degree in biotechnology, biochemistry, biology, virology or a related discipline (BSc or MSc)
• At least 3–5 years of experience working in a science and technology–focused team within a complex (bio)pharmaceutical environment
• Familiarity with viral seed and cell line testing strategies (experience preferred but not required)
• Experience collaborating across global teams and cultures
• Strong analytical and problem-solving skills; comfortable working independently and making sound decisions in a dynamic, evolving environment
• Understanding of global regulatory and compliance requirements for seeds
• Clear and effective communication skills in English

What we offer

We welcome you to a truly global, dynamic and challenging environment with great opportunities for personal development. Our benefits are very competitive, and the summary below will give you an idea of what you can expect.

• Competitive salary and a 3% year-end allowance;
• 35,5 days of leave;
• Attractive collective health care insurance package with considerable reduction rates;
• Solid Pension Plan;
• Annual bonus based on own and company performance;
• Travel allowance for commuting;
• Numerous training, coaching and e-learning modules for long term job opportunities and development.

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.

For questions about this vacancy

Please send an email including the vacancy number and job title to the following email address: RecruitmentNL@MSD.com.

Required Skills:

Aseptic Manufacturing, Audits Compliance, Cell Cultures, Cell Seeding, Corrective and Preventive Action (CAPA), Detail-Oriented, Documentation Review, Driving Continuous Improvement, GMP Compliance, Microbial Biotechnology, Microbiology, Pharmaceutical Microbiology, Quality Assurance Tools, Quality Management Systems (QMS), Quality Standards, Regulatory Affairs Compliance, Root Cause Analysis (RCA)

Preferred Skills:

Biotechnology, Pharmaceutical Industry, Science

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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:

Project Temps (Fixed Term)

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

11/25/2025

*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.