Production Specialist


Valais
Permanent
Negotiable
Manufacturing
PR/580683_1771596356
Production Specialist

We are currently partnering with a rapidly expanding pharmaceutical organization seeking a dedicated Production Specialist to strengthen their Drug Product manufacturing team in Switzerland. This role offers an excellent long‑term career path within one of the most dynamic and fast‑growing CDMOs worldwide.

You will be responsible for:

  • Performing full end‑to‑end Drug Product manufacturing activities in a GMP‑regulated environment, including batch execution, documentation, deviation support, and review of results
  • Maintaining accurate and compliant GMP records such as batch documentation, logbooks, and forms, while assisting with process updates and CAPA‑related tasks
  • Ensuring each batch is manufactured safely, on schedule, and in accordance with quality and aseptic requirements
  • Preparing, operating, and cleaning equipment used for liquid and lyophilized vial production
  • Supporting formulation and compounding steps, buffer/media preparation, equipment washing and sterilization, filter integrity testing, aseptic filling/crimping, and visual inspection
  • Contributing expertise in aseptic handling within isolators or traditional cleanroom setups; experience with single‑use technology is highly beneficial
  • Training colleagues and offering technical support across multidisciplinary teams
  • Identifying equipment abnormalities and working closely with engineering teams on repairs within classified areas

An ideal candidate should have the following qualifications:

  • 2-4 years of hands‑on GMP manufacturing experience, ideally in sterile Drug Product or Fill & Finish operations
  • Background in Drug Product manufacturing is a strong advantage; EFZ apprenticeship (e.g., mechanic, production mechanic, automotive mechanic) or experience in roles with strict hygiene standards (e.g., culinary professions) is also valued
  • Good English skills for daily instructions and communication; German knowledge is an additional asset
  • Understanding of GMP requirements, SOPs, and quality‑driven workflows
  • Reliable, structured, and collaborative approach to teamwork
  • Basic IT proficiency; SAP/MES experience is a plus
  • Willingness to participate in limited on‑call support
  • Availability to work in a 2‑shift model and readiness to transition to a 3‑shift system (regular weekday operations with occasional Saturdays, no Sundays)

What We Offer:


* Competitive compensation
* A chance to contribute to impactful projects and grow professionally within a thriving organization

If this opportunity interests you, please apply!


NOTE: Only shortlisted candidates will be contacted. Only individuals with the legal right to work in Switzerland can be considered (e.g., EU citizens or holders of a valid Swiss work permit).

FAQs

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