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Job Description We are excited to announce the job opening for an Associate Director (m/f/d) Analytical Transfer Lead to lead and execute analytical transfer activities on Monoclonal Antibodies from R&D to an internal Manufacturing site or to an contract manufacturing organization (CMO). This position should be ideally located in Boxmeer (the Netherlands) or Unterschleißheim (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 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: Hybrid Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 06/24/2026 *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.
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