* 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
#J-18808-Ljbffr