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Manufacturing Process Expert – Drug Product 80-100% (f/m/d)

Lonza·Visp·23.09.2026

 lonza.com

 
 
full_time80–100%
Job written in
English
Location
Visp
Work type
On-site
Type
Full-time

 

Lonza, a global leader in life sciences, is seeking a Manufacturing Process Expert, Drug Product to join their team in Visp, Switzerland. The company operates across five continents, focusing on innovative solutions that improve lives. They value their employees' ideas and contributions, fostering a culture of ownership and impact. The Manufacturing Process Expert, Drug Product will support the manufacturing team, engineers, and QA operations. They will troubleshoot processes, ensure compliance with cGMP guidelines, and drive improvement projects. The role involves executing manufacturing activities, evaluating batch data, and resolving issues. The expert will also handle production documentation, investigations, and process changes. Training activities and serving as a resource to other departments are also part of the responsibilities. Candidates must have a Bachelor's or Master's degree in Pharmaceutical Technology, Chemistry, Pharmacy, or a related scientific field. They need 3-5 years of experience in Sterile Manufacturing, with a focus on operations. Proficiency in English is required, and knowledge of German is beneficial. Familiarity with GMP requirements, quality procedures, and SOP execution is essential. Strong communication skills and a proactive, well-organized working attitude are also crucial. Experience in QA is advantageous. The role offers a dynamic working culture, an ethical workplace, and a variety of benefits. The team is motivated and inclusive, with a focus on continuous improvement. The location provides an up-to-date production line and an agile career path. What the role asks for: - Bachelor- or Master's degree in Pharmaceutical Technology, Chemistry, Pharmacy or an equivalent scientific field. - 3-5 years of experience in Sterile Manufacturing in Production. - Fluently English. - Knowledge of GMP requirements, quality procedures and SOP execution. - Structured, focused, proactive and well-organized work approach. - Flexibility in working hours.

 

 

 

 

 

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