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
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
If this sounds like you, don’t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter : .
Senior Manufacturing Associate. • Mittelland
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