Manufacturing Associate (Aseptic & Cell Culture)

Randstad - High priority

Luterbach

On-site

CHF 70,000 - 100,000

Full time

44 hours ago
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Job summary

Randstad is supporting a leading biotechnology company in Luterbach, Solothurn, in hiring a Manufacturing Associate. The role requires performing and documenting daily manufacturing operations in a cGMP environment, including operation of process equipment and adherence to validation protocols.

You will maintain training levels, support on-site operations, and ensure compliance with cGMP while maintaining equipment and facilities.

Qualifications

  • 3–5 years of relevant pharma/biotech experience.
  • Experience with aseptic techniques and cell culture under Biosafety Cabinets.
  • Excellent English communication skills.
  • Strong attention to detail and documentation.

Responsibilities

  • Performs and documents daily manufacturing operations in a cGMP environment.
  • Operates process equipment and executes validation protocols.
  • Maintains cGMP compliance and keeps equipment and facilities in good condition.
  • Supports on-site operations and collaborates with other functions.

Skills

Aseptic techniques
Documentation
English communication
Attention to detail

Job description

Jobdescription

For our client, a leading biotechnology company, we are seeking aManufacturing Associate.

General Information:
  • Start date:ASAP
  • End date: 28.02.2027
  • Extension: to be discussed
  • Workplace:Luterbach, Solothurn
  • Workload:100%
  • Working hours:Standard, Monday - Friday, (requires rotational weekend coverage), no shifts
Tasks & responsibilities:
  • Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents.
  • Ensuring compliance to cGMP as well as maintaining equipment and facilities.
  • Maintaining training level to the required level and support other functions on site.
  • Assists with daily manufacturing operations in manufacturing facility.
Requirements:
  • 3-5 years of relevant experience, ideally in pharma or biotech environment
  • Experience with aseptic techniques and cell culture operations under Biosafety Cabinets (BSC)
  • Excellent communication skills in English
  • Attention to details with strong documentation skills
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