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QA Specialist - External Manufacturing 100% M/F

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Employment type
Temporary
Workload
100%
Location
Boudry
Languages
French, French
First posted
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  • 14 octobre 2026
  • 100%
  • Temporary
  • Boudry

ALBEDIS is a leading Swiss recruitment partner, specializing in connecting talent and companies across a wide range of sectors, from support positions to management functions. A member of Interiman Group, ALBEDIS relies on the combined expertise of its partner brands to cover areas such as architecture and real estate, finance, IT, life sciences, legal, or human resources, with a presence throughout Switzerland (Berne, Genève, Lausanne, Zurich).

Quality Assurance Specialist - External Manufacturing 100% M/F #

Company Description ##

Our client is a leading international pharmaceutical company located in the Neuchâtel region. To support its Quality Operations team, we are looking for an experienced

Quality Assurance Specialist - External Manufacturing 100% M/F

Job Description ##

  • Act as the main Quality Assurance contact for external manufacturing partners and ensure effective quality supervision.
  • Review and approve deviations, change controls, investigations, complaints, and batch documentation.
  • Coordinate product release activities and guarantee compliance with GMP and regulatory requirements.
  • Drive the resolution of quality and operational problems while respecting commercial deadlines.
  • Collaborate closely with supply chain, manufacturing, and regulatory teams to support product availability and distribution.
  • Monitor quality indicators, identify risks, and drive continuous improvement initiatives.
  • Support audits, inspections, and quality system activities with internal and external stakeholders.

Profile Sought ##

  • Bachelor's or Master's degree in Life Sciences, Pharmacy, Biotechnology, or a related scientific field.
  • Minimum 3 years of experience in Quality Assurance in the pharmaceutical industry.
  • Mandatory experience in sterile manufacturing environments.
  • Strong knowledge of GMP regulations and pharmaceutical quality systems.
  • Proven ability to coordinate multiple stakeholders, manage priorities, and provide solutions within tight deadlines.
  • Excellent analytical, problem-solving, and communication skills.
  • Proficiency in English; French and/or German are strong assets.

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Posted 1 week ago

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