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Client:
Swisslinx
Location:
Job Category:
Manufacturing
Job Reference:
8ca738cda941
Job Views:
9
Posted:
21.01.2025
Expiry Date:
07.03.2025
Job Description:
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, Swiss, salary.
If this sounds like you, don’t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter.
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