CQV Engineer / Qualification & Validation Engineer 80-100% (m/f/d)

We are seeking a CQV Engineer / Qualification & Validation Engineer (80‑100 %) for Lonza's Visp facility. In this position you will organise, carry out and record qualification and validation tasks for equipment, systems and processes, ensuring full compliance with GMP and relevant regulatory guidelines. Your everyday duties involve drafting and reviewing protocols, conducting risk assessments, and working closely with engineering, operations and quality teams to deliver traceable, compliant documentation for both new installations and existing production lines. The successful candidate holds an engineering degree, ideally in chemical, mechanical or pharmaceutical engineering, and brings three to five years of practical CQV experience within the life‑science sector. You should demonstrate solid project‑management capabilities, be comfortable analysing data, and possess clear communication skills to interact effectively across functions. The role offers the chance to contribute to cutting‑edge biopharmaceutical manufacturing in a global, innovative environment, directly supporting the delivery of therapies that improve patient outcomes. What the role asks for: - Engineering degree (chemical, mechanical or pharmaceutical) - 3‑5 years hands‑on CQV experience in life‑science industry - Strong project‑management skills - Strong data‑analysis skills - Strong communication skills