Manufacturing Associate II.

job details

summary.

  • specialism
    life sciences
  • contact
    Walentyna Dobrowolska
  • reference number
    23353

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job details
For our client, a leading biotechnology company, we are looking for a Manufacturing Associate II to support upstream processing.


General Information:
  • Start date: ASAP
  • End date: 31.01.2026, with the possibility of extension.
  • Workplace: Luterbach, Solothurn
  • Workload: 100%
  • Remote/Home office: Not available

About the job:

As a Manufacturing Associate (MA), you will perform and document daily manufacturing operations in a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, revising cGMP documents, ensuring compliance with cGMP standards, and maintaining equipment and facilities. The MA is detail-oriented with strong documentation skills and must maintain the required training level to support other functions on site.

Tasks & Responsibilities:
  • Execute manufacturing processing steps and/or support activities, ensuring alignment with recipe & MFG documentation.
  • Troubleshoot and investigate equipment and process issues.
  • Revise documents and manage equipment/process changes.
  • Participate in training activities and manage your individual training plan; train other associates as required.
  • Execute validation protocols.
  • Lead shifts in the absence of the supervisor and facilitate shift exchanges.
  • Coordinate activities and daily schedules with cross-functional teams.
  • Perform other duties as assigned from time to time.

Must haves:
  • High school diploma and 3-5 years of relevant experience with Upstream Processing in Pharma / Biotech Production.
  • Languages: English (B1), German and/or French is a plus.
  • Understanding of the Biotech process (upstream) and ability to follow written procedures and protocols.
  • Solid knowledge of documentation requirements in a cGMP environment.
  • Trained and skilled in operational and regulatory procedures of at least one manufacturing department.
  • Basic understanding of automation or comfort with technology platforms.
  • Ability to document and record job-related information independently.
  • Strong verbal and written communication skills.

Sounds like a great opportunity for you? Apply now! We look forward to receiving your application!
For our client, a leading biotechnology company, we are looking for a Manufacturing Associate II to support upstream processing.


General Information:
  • Start date: ASAP
  • End date: 31.01.2026, with the possibility of extension.
  • Workplace: Luterbach, Solothurn
  • Workload: 100%
  • Remote/Home office: Not available

About the job:

As a Manufacturing Associate (MA), you will perform and document daily manufacturing operations in a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, revising cGMP documents, ensuring compliance with cGMP standards, and maintaining equipment and facilities. The MA is detail-oriented with strong documentation skills and must maintain the required training level to support other functions on site.

Tasks & Responsibilities:
  • Execute manufacturing processing steps and/or support activities, ensuring alignment with recipe & MFG documentation.
  • Troubleshoot and investigate equipment and process issues.
  • Revise documents and manage equipment/process changes.
  • Participate in training activities and manage your individual training plan; train other associates as required.
  • Execute validation protocols.
  • Lead shifts in the absence of the supervisor and facilitate shift exchanges.
  • Coordinate activities and daily schedules with cross-functional teams.
  • Perform other duties as assigned from time to time.

Must haves:
  • High school diploma and 3-5 years of relevant experience with Upstream Processing in Pharma / Biotech Production.
  • Languages: English (B1), German and/or French is a plus.
  • Understanding of the Biotech process (upstream) and ability to follow written procedures and protocols.
  • Solid knowledge of documentation requirements in a cGMP environment.
  • Trained and skilled in operational and regulatory procedures of at least one manufacturing department.
  • Basic understanding of automation or comfort with technology platforms.
  • Ability to document and record job-related information independently.
  • Strong verbal and written communication skills.

Sounds like a great opportunity for you? Apply now! We look forward to receiving your application!

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Walentyna Dobrowolska

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