Manufacturing Associate II

vor 1 Woche

Luterbach, Schweiz Randstad (Schweiz) AG Vollzeit

For our client, an international company in Solothurn, we are looking for a Manufacturing Associate II.


General Information:

  • Start date: 01.02.2025
  • End date: 31.01.2026
  • Extension: Possible
  • Workplace: Solothurn
  • Workload: 100%
  • Remote/Home office: Not available

Job Summary:

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. The MA is detail-oriented with strong documentation skills. Maintain training level to the required level and support other functions on site.


Tasks & Responsibilities:

  • Execute manufacturing processing steps and/or manufacturing support activities, monitoring the process against the recipe & MFG documentation.
  • Perform troubleshooting/investigation of equipment and process issues.
  • Revise documents as instructed and manage equipment and/or process changes.
  • Actively participate in training activities, managing their individual training plan, train other associates as required.
  • Execute validation protocols.
  • Lead shifts when the supervisor is absent, and actively leads or participates in shift exchanges.
  • Coordinate activities and daily schedules with cross-functional teams.
  • Perform other job duties as assigned.

Must haves:

  • High school diploma or equivalent experience and typically 3-5 years of relevant experience in related / non-related industry or 2-3 years of experience in Pharma/Biotech industry.
  • Bachelor’s degree in a related field with 1-2 years of professional experience; or a Bachelor’s degree in a non-related field with 3-4 years of experience.
  • Languages: English B1, German and/or French an asset.
  • Basic understanding of the Biotech process, able to follow and comply with written procedures and protocols.
  • Solid understanding of the requirements within correct and timely documentation within a cGMP environment.
  • Trained and skilled in all operational and regulatory procedures of at least one manufacturing department.
  • Basic understanding of automation or comfort with technology platforms.
  • Ability to independently document and record job-related information.
  • Good verbal and written communication skills.

If this sounds like you, we’d love to hear from you Submit your CV today and join a leading pharmaceutical company driving innovation.

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