cGMP Manufacturing Specialist III – Night Shift

Experis Switzerland

Bezirk Solothurn

Vor Ort

CHF 60.000 - 90.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

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Zusammenfassung

Experis Switzerland is seeking a Manufacturing Associate for a 5-shift rotation including nights in Luterbach, Solothurn. Start date 21.09.2026; end date 28.02.2027.

The role requires 3–5 years of experience in a cGMP environment, strong documentation, and the ability to work independently while collaborating with on-site teams. You will be responsible for daily manufacturing operations, equipment maintenance, and ensuring compliance with health, safety, and environmental regulations.

Qualifikationen

  • 3–5 years of experience in manufacturing.
  • Experience in a cGMP environment and operation of process equipment.
  • Strong documentation skills and training maintenance.
  • Ability to work independently with minimal direction.
  • Good verbal and written communication skills.
  • Commitment to safety and EH&S regulations.
  • Maintain training curriculum and follow procedures.

Aufgaben

  • Perform and document daily manufacturing operations in a cGMP environment.
  • Operate process equipment and execute validation protocols.
  • Maintain equipment and facilities and ensure regulatory compliance.
  • Maintain training levels and support other functions on site.
  • Collaborate with supporting functions to achieve best outcomes for patients and the facility.
  • Demonstrate accurate documentation and record-keeping for all activities.
  • Consult supervisor or manager when in doubt and communicate issues clearly.
  • Ensure adherence to safety principles and regulatory procedures.

Kenntnisse

Detail-oriented
Documentation
Independent worker
Verbal communication
Written communication
Collaborative
Biopharmaceutical knowledge

Jobbeschreibung

Experis Switzerland is seeking a Manufacturing Associate for a 5-shift rotation including nights in Luterbach, Solothurn. Start date 21.09.2026; end date 28.02.2027.

The role requires 3–5 years of experience in a cGMP environment, strong documentation, and the ability to work independently while collaborating with on-site teams. You will be responsible for daily manufacturing operations, equipment maintenance, and ensuring compliance with health, safety, and environmental regulations.

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