Process Validation Specialist
Key information
- Publication date:29 April 2025
- Workload:100%
- Contract type:Temporary
- Place of work:Valais
Our Gi Life Sciences team recruits a Process Validation Specialist for our client based in the canton of Valais.
Long-term temporary position
Start date : ASAP
Key responsibilities:
- Definition of the validation strategy. (study design / drafting of protocols and reports).
- Preparation of risk analyses.
- Support R&D teams during the process characterization phase.
- Review and approval of process characterization documents.
- Intervention on pharmaceutical process validation projects.
- Responsibility for the evaluation of change and variance validation (approval of changes and variances).
- Preparation and maintenance of a detailed plan for ongoing process verification.
- Assessment and approval of product quality reviews.
Key requirements:
- You have a degree in chemistry, biology, biotechnology, chemical engineering or equivalent.
- You have first-time experience in project management, preferably in operations, MSAT, quality and compliance. (interaction with regulatory bodies a strong asset).
- You have a first experience in mammals.
- Good ability to manage multiple tasks within the given time frame.
- You are fluent in English. Knowledge of German will be highly appreciated.
Contact
- Jessica LiuzzoWrite an email