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As an Associate / Senior Associate Non-GMP Manufacturing, you are part of the Global Drug Product Process Engineering and Manufacturing group in Pharmaceutical Development in Basel, Switzerland. The department Pharmaceutical Development is responsible for the development of parenteral drug products from Phase 1 up to Launch. Activities of the NonGMP Manufacturing group encompass DP manufacturing for technical and GLP Tox studies to supply Roches pipeline projects.

Manufacturing  and aseptic handling of non-GMP formulations / products (eg for parenteral biologics, peptides or small molecules)

Preparation of primary packaging and equipment, compounding, sterile filtration, aseptic filling (vial, PFS, cartridges) visual inspection as well as performing of in-process controls 

Responsible for the diligent cleaning of equipment and performing and overseeing batch-related and routine microbiological monitoring

Collaborate with project leads to define filling requirements and translate them into a product-specific batch record in document management systems (e.g. Benchling) according to relevant guidance and internal process 

Optimization of process equipment and processes and evaluation and implementation of new technologies and support the commissioning of new equipment, including SAT execution, creation of SOPs , and performing of OQ activities

Contribute to the organizational development of the Drug Product Process Engineering and Manufacturing group
 

You are a motivated candidate with excellent technical, communication and organizational skills, fully committed to team effort but able to work in an independent fashion. Further you bring:

Completed vocational training as a Chemical or Biological Laboratory Technician, Pharmaceutical Technical Assistant, Chemical Technical Assistant, Biological Technical Assistant or equivalent and/or BSc in a life science discipline (e.g. biology, biotechnology, pharmacy, chemistry or equivalent)

3+ years of relevant  professional experience  in the field of aseptic manufacturing

Hands-on lab experience including eg preparation and sterilization of materials, compounding, microbiological monitoring , performing in-process controls

Good organization and planning skills combined with the ability to work independently and take ownership of assigned tasks

Willingness to support team members when needed and contribute to a collaborative work environment

Good oral and written communication skills in German and English

Sounds like you? We are looking forward to receiving your application by 23 September 2025.

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.