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Technical Lead MSAT

Technical Lead MSAT

Reference: BBBH28912
Date posted: 23/03/2026
Job details
Specialism
Technical Operations
Expertise
Discovery/R&D
Location
Basel, Basel-City, Switzerland
Job type
Contract
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Description

Ready to engineer precision in the world of biotech? Join our client’s cutting-edge team and play a vital role in developing the instrumentation that powers tomorrow’s breakthroughs.

R&D Partners is seeking a Technical Lead MSAT to support manufacturing and analytical processes for small molecule drug products. This role focuses on ensuring reliable, cost-effective, and compliant production for clinical and commercial use. You will act as a subject matter expert, lead technical projects, and collaborate with external manufacturers to optimize processes and introduce innovative solutions.

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

Responsibilities:

  • Act as an expert in small molecule drug product manufacturing.
  • Oversee process validation and ensure compliance with regulatory standards.
  • Support external manufacturing activities, including addressing process changes, deviations, and risk assessments.
  • Review and approve procedures, manufacturing instructions, and technical documentation.
  • Contribute to setting up and updating analytical specifications and stability programs.
  • Write and review sections of regulatory filings and annual product reviews.
  • Lead technical projects, such as process improvements and cost optimization.
  • Evaluate and support new contract manufacturers and participate in supply and quality agreement development.
  • Manage product transfers, scale-up activities, and validations at external manufacturing sites.
  • Stay updated on advancements in biopharmaceutical manufacturing technologies and assess their applicability.

Key Skills and Requirements:

  • Background in Chemistry, Pharmacy, or a related field.
  • Strong knowledge of small molecule drug product manufacturing and CMC development.
  • Experience working in cross-functional teams and managing multiple priorities.
  • Familiarity with regulatory guidelines and documentation processes.
  • Excellent communication skills, both written and verbal.
  • Fluent in English.
  • Ability to work independently, take initiative, and collaborate effectively.

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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