Associate Director (m/f/d) Analytical Transfer Lead

Job Description

We are excited to announce the job opening for anAssociate Director (m/f/d) Analytical Transfer Leadto lead and execute analytical transfer activities onMonoclonal Antibodies from R&D to an internal Manufacturing site or to an contract manufacturing organization (CMO).

This position should be ideally locatedin Boxmeer (the Netherlands) orUnterschleißheim (Germany). The position will require up to 25% international travel.

Your Key Responsibilities:

• Lead and execute analytical transfer projects (setting up and execution of transfer plans, resource needs, and timeline adherences) for both drug substance and drug products
• organize analytical activities in a pharmaceutical GMP and Quality Control (QC) environment;  
• coordinate & mentor ATS (Analytical tech solutions) colleagues remotely to ensure governance of several Monoclonal Antibody projects
• Collaborates with R&D,  Quality, Regulatory Affairs, external suppliers and division site responsible teams in transfer activities
• Supports strategic transfer initiatives like standardizing transfer processes and develop appropriate documentation templates
• Build up communication and trust with internal and external partners as well as stakeholders

Your Profile:

• Master, Bachelor, Engineer degree and long year experience in a Pharmaceutical/Chemical/Analytical Science required
• At least 8 years’ experience in the research and development, manufacturing and testing of active pharmaceutical ingredients (APIs) or drug products required
• Experience in analytical transfer activities and broad understanding of analytical platforms like pharmaceutical analyses (chromatography and physicochemical testing, immunosorbent assays) is an advantage
• End to end understanding of pharmaceutical business relationships and the ability to work in cross functional teams, being able to create a target focused approach
• Solid experience working in international project teams
• Ability to work independently and make decisions within guidelines and policies that impact own priorities to meet deadlines
• Proficient in scientific/technical writing and current computer usage

Be part of a collaborative, international team. This position offers significant opportunities for learning and advancement.

We look forward to your application. Don't hesitate to reach out with questions.

Required Skills:

Adaptability, Adaptability, Aseptic Processing, Assay, Biochemical Analysis, Biochemical Assays, Cell-Based Assays, Chemometrics, Chromatography, Column Chromatography, Cross-Cultural Awareness, Cross-Functional Collaboration, Customer-Focused, Driving Continuous Improvement, Freeze Drying, GMP Compliance, Immunoassays, Immunoprecipitation, Lean Six Sigma Process Improvement, Manufacturing Quality Control, Monoclonal Antibodies, Pharmaceutical Microbiology, Process Improvements, Regulatory Compliance, Risk Management {+ 1 more}

Preferred Skills:

Current Employees applyHERE

Current Contingent Workers applyHERE

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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:

06/24/2026

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