Your Role: Compliance Specialist
About the Project
Our compliance team has identified a significant opportunity to enhance compliance and efficiency by redefining and reorganizing our GMP documentation and training. To achieve this, we need to redesign and restructure our standard operating procedures (SOPs) to ensure they are aligned and optimized.
About You
* Rélevant diploma in Life-science, engineering or pharmacy (Master - ongoing)
* Knowledge in Biotechnological sciences is a plus
* Fluently spoken and written English and French
* Good editorial and communication skills
* Ability to synthesize effectively
* Autonomous
You will be working with us for 6-12 months in Aubonne, Switzerland, helping us redefine and reorganize our GMP documentation and training. This project will give you insight into all processes and tasks required to define and regulate a fully GMP compliant packaging operation. You will also understand the importance of optimization and efficiency, which must go hand-in-hand with GMP to guarantee patient safety and optimize business potential.