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QA Expert Senior

Job in 2000, Neuchâtel, Neuchâtel, Switzerland
Listing for: JobCourier
Full Time position
Listed on 2026-02-28
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, QA Specialist / Manager
  • Pharmaceutical
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 30000 - 80000 CHF Yearly CHF 30000.00 80000.00 YEAR
Job Description & How to Apply Below

Services

The objective of this resource within the Quality Ops organization is to provide support as a Quality Assurance Senior Expert in the frame of implementation of a new Fill and Finishing. He/she could also be involved in routine GMP operations for Fill and Finishing area. He/she must ensure the quality of information reported within the various systems and documentation with respect to current guidelines, compliance and regulatory requirements.

  • Approve on the floor aseptic interventions performed by manufacturing during Aseptic Process Simulation.
  • Review Master Batch Records.
  • Attend all meetings relevant to perform the above‑mentioned tasks.
  • Respect the escalation process.
  • Other tasks related to conventional quality oversight might be occasionally requested to support the team (e.g. continuous improvement initiatives, GMP tour in classified areas, etc.).
Profil recherché
  • Formation académique technique et scientifique (bac +5)
  • 2?3 d'expériences opérationnelles cGMP dans un département Qualité Ops sur un site de production Pharmaceutique de produits stériles injectables.
  • Connaissances holistiques des procédés de production (de la culture cellulaire à la répartition aseptique) : étapes unitaires, équipements, gowning, contrôles d'environnement, tests laboratoires physicochimiques et biologiques, etc.
  • Connaissance des référentiels Qualité (cGMP) et des Systèmes Qualité (Déviations, CAPA, Change Control, Training, Documentation, etc.)
  • Capacité rédactionnelle pour des documents en français et/ou anglais
  • Langues : français et anglais
  • Travail sur PC et connaissances pack Microsoft
  • Travail en équipe
  • Agilité et autonomie
Mode de travail
  • Minimum 4 jours sur site
  • Reporting au QA manager, mais travail en interaction quotidienne avec Manufacturing, Engineering, Sterility Assurance, Quality Ops, Training, etc.
  • Horaire de 2
    * 8 à prévoir pendant les tests de simulation aseptique

If you are interested, please apply with a copy of your CV at the earliest.

This job will halt to accept applications end of February.

Interviews will be online and 2 rounds.

Settore:
Industria farmaceutica

Ruolo:
Risorse umane

#J-18808-Ljbffr
Position Requirements
10+ Years work experience
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