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Packaging Engineer / Packaging Technical Lead (Pharma)

Michael Page·Zürich·02.10.2026

 michaelpage.ch

 
 
temporary80–100%
Required language
English professional
Job written in
English
Location
Zürich
Work type
On-site
Type
Temporary

 

The role is a Packaging Engineer / Packaging Technical Lead (Pharma) at a pharmaceutical company. The company focuses on ensuring compliance, efficiency, and product quality in packaging engineering activities. The main day-to-day responsibilities include managing packaging-related documentation, developing and approving technical profile drawings, and leading the qualification and implementation of new packaging components. The role also involves supporting packaging process validation, managing change controls, and coordinating the implementation of packaging platform components globally. Additionally, the role supports product launches, lifecycle management, and continuous improvement projects. The must-have requirements include a Bachelor's Degree in Engineering, Packaging Engineering, or a related technical discipline, and a minimum of 5 years of experience within the pharmaceutical industry or a similarly regulated environment. Strong knowledge of cGMP requirements and pharmaceutical documentation practices is essential. Fluency in English and mandatory experience with TrackWise are also required. Nice-to-have skills include experience with Veeva or similar document management systems. The role involves collaborating with various departments and external partners, driving projects independently, and understanding their broader strategic and business impact. What the role asks for: - Bachelor's Degree in Engineering, Packaging Engineering, or a related technical discipline. - 5 years of experience within the pharmaceutical industry or a similarly regulated environment. - Strong knowledge of cGMP requirements and pharmaceutical documentation practices. - Fluency in English. - Mandatory experience with TrackWise. - Experience managing technical drawings, packaging specifications, and design changes. - Strong knowledge of electronic quality management systems. - Experience with Veeva or similar document management systems (nice-to-have).

 

 

 

 

 

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