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Senior Expert Biopharmaceutical Manufacturing (m/f/d)

Senior Expert Biopharmaceutical Manufacturing (m/f/d)

Reference: BBBH29286
Date posted: 26/06/2026
Job details
Specialism
Technical Operations
Expertise
Quality Control
Location
Munich, Bayern, Germany
Job type
Contract
Salary
€80.00 to €90.00
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Description

Drive the buildout of next-generation biopharma production from concept to qualification.

R&D Partners is seeking a Senior Expert in Biopharmaceutical Manufacturing to support the buildout of a new ADC (Antibody-Drug Conjugate) production area. This role requires a strong background in GMP manufacturing, cleanroom establishment, and single-use system integration, with a focus on technical oversight during construction and commissioning phases.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Provide deep alignment with the ADC buildout scope, ensuring seamless project execution.
  • Oversee cleanroom establishment, single-use system integration, and technical readiness during construction and commissioning.
  • Lead GMP manufacturing activities, including downstream processing, bioconjugation workflows, TFF, UF/DF filtration, and disposable production systems.
  • Manage commissioning, qualification, and validation processes for equipment startup, facility readiness, and end-to-end qualification activities.
  • Develop and maintain GMP documentation, including SOPs, work instructions, manufacturing instructions, and risk assessments.
  • Collaborate in interdisciplinary project environments, driving implementation, knowledge transfer, and cross-functional alignment.
  • Communicate effectively in English and German with global teams, ensuring clarity across engineering, QA, validation, and operations stakeholders.

Key Skills and Requirements:

  • Extensive hands-on experience in GMP manufacturing and downstream processing.
  • Proven expertise in commissioning, qualification, and validation for new production areas.
  • Strong command of GMP documentation and compliance frameworks.
  • Solution-oriented approach with the ability to drive implementation in complex project environments.
  • Availability for a 5-day onsite working pattern with 20% remote flexibility and required travel.
  • Fluent in English and German.

For more information, please contact Jessica Taylor.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/

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Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

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