Engineering Associate - Validation & Compliance

for a pharmaceutical company in the canton of Neuchâtel, our team is actively looking for an Engineering - Compliance - Temporary contract Start date: June 1 End date: February 1 Main mission Ensure the implementation, execution, and activities of (C&Q) and periodic reviews of GMP equipment and systems. Key Responsibilities Carry out periodic reviews of equipment and systems, keep risk assessments updated, and integrate new equipment into the process. Participate in C&Q activities: document review and execution, prepare and optimize the periodic review process (frequency, criticality, workload, document templates). Propose improvements and optimize the performance of the system. Contribute to the writing and updating of local procedures. Apply existing procedures (BMS). Interact with various departments on site (Quality, Production, Engineering ). Profile sought Engineering degree in biology, biochemistry, quality, or equivalent experience in risk analysis and good knowledge of regulatory requirements. Proficient in Microsoft Office tools. Excellent analytical and writing skills. Autonomy, rigor, dynamism, and ability to propose solutions. Fluency in French and English required. Contact Gi Life Sciences: jid236d256aen jit0207aen jpiy26aen