C&Q Lead (Pharma / Biotech)

Main tasks:

The C&Q lead will be in charge of the implementation, commissioning and qualification of process equipment (USP & DSP) on major biotechnology sites :

• Perform design gap checks (URS, Functional Specifications)
• Lead the planning, execution, and documentation of commissioning and qualification activities 
• Collaborate with engineering, quality, and production teams to define commissioning and qualification strategies that align with project timelines and business objectives
• Develop and review protocols, test scripts, and validation documentation for process equipment
• Coordinate and oversee the execution of commissioning and qualification activities, including performance testing, installation verification, operational qualification, and performance qualification
• Identify and resolve technical issues and deviations during commissioning and qualification

Required profile:

• Master's degree in Mechanical / Electrical engineering, Life Science, Pharmaceutical production or a related field 
• 5 years minimum experience as C&Q engineer or a similar position
• Experience in the pharmaceutical / biotech / chemicals sector 
• Knowledge of USP and DSP equipment
• Fluent in French, English is a plus 
• Swiss or EU nationality, or valid Swiss working permit 

Thank you for your interest. Please note that only candidates selected for a first interview will be contacted.