We are looking for a Compliance/Validation Engineer to join the Engineering Asset Management team and support execution of CQV (Commissioning, Qualification, Validation) and engineering compliance activities, in alignment with regulatory expectations and Good Manufacturing Practices. This role is for you if you bring hands‑on experience in a pharmaceutical or biotech environment, paired with sharp analytical thinking, a keen eye for detail, and the confidence to influence and align cross‑functional teams. How you might spend your days

Authoring and reviewing CQV protocols, SOPs, and technical documentation, ensuring everything meets rigorous GMP standards and holds up under scrutiny Leading investigations into deviations and non‑conformances, driving CAPA implementation that gets to the root cause and keeps issues from coming back Being a trusted voice for the engineering team during internal and external audits Coordinating and executing engineering and quality change control...