Quality Assurance Engineer – Life Sciences (FR)

Prepares, executes, and finalizes protocols (IQ, OQ, PQ) for validating current, new and improved manufacturing processes.
Establish and review protocols, reports, procedures, specifications and systems to ensure the development of GMP compliant pharmaceutical products.
Conduct and lead process/design failure mode effects and analysis.
Represents the company as the point of contact with regulatory agencies, including interface with the FDA inspectors.
Behave as a leader in all areas of the Quality System.

Bachelor degree in an engineering or equivalent field. A Master’s degree is a plus.
At least 3 years of related experience in a pharmaceutical, biotechnology or a healthcare discipline is required.
Strong experience in designing verification/validation, process verification/validation, and design/process failure modes and effects analyses.
Knowledge of Good Manufacturing Practices (GMP).
Proficiency with the Microsoft Office Suite.
Fluent in French and good level of English.
Locations: Multiple options for locations in Romandy

Job info

25/03/2024

Vaud