Description

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.