Manufacturing Science and Technology Expert – Drug Product (m/f/d) 80% -100%

Lonza, a worldwide leader in life‑science solutions operating on three continents, is looking for a Manufacturing Science and Technology Expert focused on drug products. The position is based in Visp, Switzerland, with relocation support for the candidate and their family. The role is central to guaranteeing smooth technology transfers, up‑holding GMP standards and fostering ongoing process enhancements. On a daily basis the employee will introduce the manufacturing method supplied by drug‑product development or the client into the plant. They will steer technology transfers by applying structured tools to manage information flow, risk assessment and change‑control procedures. Participation in GMP risk analyses, preparation of qualification and validation work, and oversight of change‑control and deviation investigations are also expected. The expert will guide cross‑functional teams as the MSAT lead, ensuring that projects move from planning through execution to completion while meeting project‑management targets. Continuous improvement of process performance, product quality and data‑driven monitoring strategies falls within the remit, as does mentoring of scientific and production staff and acting as a liaison between Drug Product Services in Basel, QC and the Visp site. The candidate must hold a university degree in Pharmaceutical Technology, Biotechnology, Chemistry, Process Engineering or a comparable scientific discipline. At least three years of demonstrable experience in sterile manufacturing on the shop floor or within MSAT, QA/QC environments is required. Fluency in English is essential, together with a solid grasp of sterile‑manufacturing processes, relevant regulatory frameworks and freeze‑drying technology. Strong interpersonal abilities and the capacity to collaborate across customers and matrix‑structured teams are mandatory. The role also calls for an organized, focused work style that welcomes fresh ideas, as well as a proactive, highly motivated attitude geared toward solving problems. Additional qualities that will help the incumbent succeed include an open‑minded approach to new insights, a structured and detail‑oriented mindset, and a drive to resolve issues swiftly. The position offers the chance to work in a dynamic, multinational environment where scientific expertise directly contributes to products that improve millions of lives. Lonza promotes an inclusive culture, ethical conduct and respect for both people and the environment. What the role asks for: - Degree in Pharmaceutical Technology, Biotechnology, Chemistry, Process Engineering or similar - Over 3 years experience in sterile manufacturing shop‑floor or MSAT/QA‑QC - Fluent English proficiency - Proven understanding of sterile pharma processes, regulations and freeze‑drying - Excellent interpersonal and collaborative skills across customers and matrix teams - Organized, focused and receptive to new ideas - Proactive, highly motivated and strong issue‑resolution drive