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

What we offer you

At Alten, we offer you the security of a permanent contract while also giving you the liberty to work with multiple prestigious clients. With the luxury of having a wide range of offices around the world, we are in a unique position to provide you with the freedom to experience national and international business opportunities. Thus, we function in a highly innovative market, always being up to date with the latest technologies and making you a pioneer in your field. Therefore, we offer our employees sought-after trainings and workshops ranging from hard to soft skills and providing you with certificates that will further increase your qualifications, enabling you to participate in ground-breaking projects.

Apply now and be a part of our amazing journey. We believe in growing together!