GMP Manufacturing Support

☞ Randstad Switzerland

View: 133

Update day: 24-04-2024

Location: Visp Valais VS

Category: Executive management Production / Operation

Industry: Staffing Recruiting Biotechnology Pharmaceuticals

Position: Entry level

Job type: Full-time

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Job content

Do you wish to be part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative ?

For our client, this pioneering biotechnology company, we are looking for a:

GMP Manufacturing Support

Location:Visp

Contract: Temporary for one year.

Your Responsibilities
  • Work cross-functionally to assist in planning CMO activities, batch record review, deviation management, and project initiatives.
  • Perform batch record review and approval at CMO to support on time batch release.
  • Coordinate reviews and approvals of various CMO documentation as required.
  • Write or revise and approve the appropriate GMP documentations. e.g.: change request, deviations, master batch records.
  • Coordinate and support investigations and troubleshooting efforts at CMOs, in collaboration with Quality and MS&T Lead small cross-functional teams to drive manufacturing operations changes or improvements Attend daily operational meetings at the CMO.
Your Profile
  • Education: University degree in a technical discipline related to Pharmaceutical Manufacturing (e.g. Pharmacy, chemistry, biotechnology, engineering)
  • Experience: entry-level position
  • Ability to manage multiple competing priorities in a fast-paced environment
  • Strong proficiency in English. German or Spanish as an advantage.
You would like to contribute to a fast-thinking and innovative company, changing the industry ? Apply now

Please note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position
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Deadline: 08-06-2024

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