Help advance next-generation monoclonal antibody processes within a global Centre of Excellence. Join our team in Boxmeer as a Scientist – Monoclonal Antibody Process Development, supporting the Centre of Excellence for Monoclonal Antibodies (CoE mAb) within the Bioprocess Technology Solutions department of Animal Health.
About the RoleAs a Scientist, you will design, plan, and execute cell‑culture experiments in bioreactors (upstream processing – USP) and monoclonal antibody purification and formulation activities (downstream processing – DSP). You will also take on basic project leadership responsibilities in the development of new mAb products, improvement of existing products, and resolution of production‑related challenges both within facilities and at CDMOs.
Responsibilities- Design, plan, and execute laboratory experiments (USP, DSP, and formulation) in accordance with QbD principles and project goals.
- Collaborate with project leads and cross‑functional teams to define study designs and coordinate supporting activities.
- Analyze, interpret, and document experimental results; share insights and contribute to data‑driven decision‑making.
- Identify deviations, investigate root causes, and recommend improvements to processes, methods, or study designs.
- Prepare clear and concise technical documentation, such as protocols, reports, and memos, in English.
- Perform all activities in compliance with GxP, safety (EHS), and quality standards, including support for pilot and production‑scale work.
- Contribute to continuous improvement by proposing and implementing new methods, technologies, or workflows.
- Support team and departmental objectives, including equipment lifecycle management, onboarding/training, and participation or leadership in small projects.
- Bachelor’s or Master’s degree in biotechnology, bioprocess technology, or a related field (Master’s preferred).
- Relevant hands‑on industry experience in mAb process development, preferably 5 years working with bioreactors and/or purification and formulation.
- Working knowledge of laboratory setup, operations, and regulatory requirements.
- Proficiency in English, both written and spoken.
- Experience with GxP guidelines and compliant ways of working.
- Familiarity with Manufacturing Process Sciences (MPS) methods and practices.
- 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.
- High‑quality company restaurant with fresh and healthy options.
- Excellent accessibility: train station adjacent to the main entrance and ample parking.
- Contribution toward personal sports membership.
- Private park on site for walking or relaxation.
- Mental well‑being support through Lyra Health for you and your family members.
- Dedicated prayer/meditation room.
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, 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 the 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.
Job Posting End Date06/3/2026
#J-18808-Ljbffr€60000 - €80000 monthly