Quality Assurance Engineer – Life Sciences (FR)

ALTEN is a leader consultancy company divided in 3 different business units: IT, Engineering and Life and Science, operating in more than 30 countries worldwide by now. We have around 54,000 employees (88% engineers) working with our clients. ALTEN group has 6,500 Clients in various sectors such as pharmaceutical sector, aerospace, telecoms, finance, energy, automotive, public sector and more… As a company we support them with their expertise. In ALTEN Switzerland we have 450 Employees and 100 clients.

Are you passionate about technology and like to take on complex technical challenges? Do you want to work in exciting projects at renowned clients? At ALTEN we believe that knowing and meeting the expectations of our consultants is a key factor in our success. Our consultants make the difference. Do you want to make the difference too?

• 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