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 systemsExperience in highly regulated industryDetail-oriented with strong understanding of automated systems and process controlsWhat's on offer
A 12-month contract at an internationally known biotechnology company.Opportunity to develop in the position and companyA competitive, Swiss, salary.If this sounds like you, don’t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter : .