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16450en
- Contract
- English
- Associate
- Research & Development
- Mittelland
- Healthcare & Life Sciences
Skills
GMP, USP, DSP, Delta V, Manufacturing, Biotech, Pharma
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On behalf of our client, an international biotechnology company, Swisslinx is seeking a dedicated Manufacturing Associate to join their team. In this role, you will perform and document daily manufacturing operations in a cGMP environment, ensuring processes are executed efficiently and in compliance with industry standards.
Location: Solothurn, Switzerland
Contract Type: Contract (1 year, with shift work)
Start Date: ASAP
Workload: 100%
Your Mission:
• Execute manufacturing processing steps and support activities, monitoring processes against approved recipes and manufacturing documentation.
• Troubleshoot and investigate equipment and process issues.
• Revise documents as directed, including implementing equipment and process changes.
• Execute and document validation protocols.
Your Background:
• Bachelor’s degree or equivalent apprenticeship with a minimum of 4 years of experience in the Pharma or Biotech industry.
• At least 4 years of hands-on experience working in a GMP-regulated environment.
• Proficiency in automated systems such as DeltaV, Syncade, or SAP.
• Strong safety and quality awareness in all aspects of work.
• Language skills: Minimum English level B1.
What’s on Offer:
• High growth potential within a leading international biotechnology company.
• Collaborative and supportive company culture.
If you’re ready to take the next step in your career and meet the above requirements, we’d love to hear from you! Apply here or contact Veronika von Mentzer, Recruiter, at veronika.nakev@swisslinx.com.
Location: Solothurn, Switzerland
Contract Type: Contract (1 year, with shift work)
Start Date: ASAP
Workload: 100%
Your Mission:
• Execute manufacturing processing steps and support activities, monitoring processes against approved recipes and manufacturing documentation.
• Troubleshoot and investigate equipment and process issues.
• Revise documents as directed, including implementing equipment and process changes.
• Execute and document validation protocols.
Your Background:
• Bachelor’s degree or equivalent apprenticeship with a minimum of 4 years of experience in the Pharma or Biotech industry.
• At least 4 years of hands-on experience working in a GMP-regulated environment.
• Proficiency in automated systems such as DeltaV, Syncade, or SAP.
• Strong safety and quality awareness in all aspects of work.
• Language skills: Minimum English level B1.
What’s on Offer:
• High growth potential within a leading international biotechnology company.
• Collaborative and supportive company culture.
If you’re ready to take the next step in your career and meet the above requirements, we’d love to hear from you! Apply here or contact Veronika von Mentzer, Recruiter, at veronika.nakev@swisslinx.com.
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