Compliance Engineer DPS Growth Project

Create and review GMP documentation such as periodic reviews, qualification documents, and SOPs. Prepare presentation materials and organize subject matter experts (SMEs) for audits and inspections. Communicate effectively with internal inspection teams and support inspection readiness. Define, assess, and oversee GMP-relevant activities within CAPA and change management processes. Lead the full lifecycle of CAPAs and changes from creation through execution. Support re-qualification activities and ensure documentation accuracy. Represent the Engineering Lead Team by taking over delegated GMP-related duties.

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

• Bachelor’s degree or equivalent qualification in Pharmacy, Engineering, or a related technical field

• Strong experience in the pharmaceutical industry with focus on GMP and engineering environments

• Solid project management skills

• Excellent communication abilities and structured, detail-oriented working style

• Strong knowledge of GMP requirements and regulatory expectations

• Fluency in German and English (both required)

• Ability to collaborate effectively across stakeholders and act confidently as a GMP contact person