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16155en
- Contract
- English
- Associate
- Engineering & Technical Services
- Mittelland
- Healthcare & Life Sciences
Skills
manufacturing, drug production, pharmaceutical, GMP, Delta V, Syncade
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This vacancy has now expired
On behalf of our client, an international biotechnology company, Swisslinx is looking for a Manufacturing Associate. This is initially a 12 months contract position (extension possible) with a great opportunity to bring your proven knowledge and expertise in pharmaceutical manufacturing to an organization that offers a dynamic working environment.
Contract type - Contract
Start Date - As soon as possible
Location - Solothurn
Workload - 100%
Duration - 12 months (extension possible)
Your mission:
- Perform and document daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation
- Ensure compliance to cGMP as well as maintaining equipment and facilities
- Maintain training to the required level and support other functions on site
- Execute manufacturing related work as per procedures and policies
Your background:
- 5+ years’ experience in pharmaceutical drug substance manufacturing roles.
- Conversational English language (B1 minimum).
- Exposure to Delta V or Syncade or similar automated systems
- Experience in highly regulated industry
- Detail-oriented with strong understanding of automated systems and process controls
What's on offer
- A 12-month contract at an internationally known biotechnology company.
- Opportunity to develop in the position and company
- A competitive salary plus shift allowance.
If this sounds like you, don’t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter: hugo.palejowski@swisslinx.com.
Contract type - Contract
Start Date - As soon as possible
Location - Solothurn
Workload - 100%
Duration - 12 months (extension possible)
Your mission:
- Perform and document daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation
- Ensure compliance to cGMP as well as maintaining equipment and facilities
- Maintain training to the required level and support other functions on site
- Execute manufacturing related work as per procedures and policies
Your background:
- 5+ years’ experience in pharmaceutical drug substance manufacturing roles.
- Conversational English language (B1 minimum).
- Exposure to Delta V or Syncade or similar automated systems
- Experience in highly regulated industry
- Detail-oriented with strong understanding of automated systems and process controls
What's on offer
- A 12-month contract at an internationally known biotechnology company.
- Opportunity to develop in the position and company
- A competitive salary plus shift allowance.
If this sounds like you, don’t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter: hugo.palejowski@swisslinx.com.
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