MSAT Expert

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Life Science Recruiter, specialised in Scientific

Our client based in Basel (Switzerland) is looking for a Pharma MSAT Expert to contribute to the MSAT team at the Basel site. In this role, you will manage various technical and analytical aspects related to the manufacturing and quality control of our portfolio of pharmaceutical products.

Responsibilities:

• Manage daily technical aspects and activities related to manufacturing and quality control of our pharmaceutical products (e.g., technology transfer topics, analytical topics, manufacturing process, Quality Control investigation, and troubleshooting, etc.).
• Regularly write, review, and approve technical (manufacturing/quality control) and GxP documents (e.g., protocols, reports, and instructions) to ensure cGMP, QA, and regulatory compliance at all times.
• Management of MSAT-related Change Controls.
• Provide expertise on GxP, Quality Control, and pharmaceutical manufacturing matters.
• Provide technical (manufacturing and Quality Control) support to internal stakeholders, mainly Regulatory Affairs and Quality Assurance (e.g., questions from authorities, deviations, investigations, risk assessments).
• Assess, interpret, and give guidance (internally/externally) on analytical methods and techniques related to APIs or finished products (e.g., HPLC, endotoxins, sterility, or other analytical methods).
• Act as CMC expert support (manufacturing and Quality Control) on punctual requests coming from Regulatory Affairs.
• Assure technical exchanges and follow-ups with our different external partners (CMOs, Analytical labs, API suppliers).

Requirements:

• University degree – Master’s in Life Sciences (e.g., pharmacy, pharmaceutical sciences, chemistry, biotechnology, etc.).
• Work experience and knowledge of GMP pharmaceutical manufacturing, with a strong awareness of quality assurance aspects. Quality control experience is a valuable complementary asset.
• At least 5 years of proven experience in an operational GMP pharmaceutical environment with combined expertise in manufacturing finished products (oral forms, injectables) and analytical expertise is mandatory.
• Practical experience in managing QA documents (CCs, CAPAs, investigations, etc.) derived from operational activities.
• Ability to work on several projects simultaneously: analytical thinking and organization skills are part of your key strengths.
• English is a must, French is highly desired, and any other language is a plus.

Duration: Permanent

Salary expectations: 130K + bonus

Note: you are ready to travel (approximately 5–10% of the time)

If you feel confident about this opportunity, we encourage you to apply, or to reach out to me via email at cpflieger@actalentservices.com.

Seniority level

Associate

Employment type

Full-time

Job function

Manufacturing, Project Management, and Science

Industries

Pharmaceutical Manufacturing and Biotechnology Research