At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
A healthier future drives us to innovate. At our Basel Drug Substance site, we produce high-quality pharmaceutical active ingredients in three Value Streams – Monoclonal Antibody (MAB), Antibody Drug Conjugate (ADC), and Single Use Technology (SUT) – to provide patients worldwide with medications. The Manufacturing Lab Team offers you the opportunity to independently take on varied and challenging tasks in a biological production environment. Become part of our team and actively contribute to the development and production of innovative medicines by participating in the following processes: As a support unit, you assist with the WCB thawing process. You accompany and advise interfaces on the correct technical execution of the E2E process for process samples and their analyses in the production buildings. You handle deviations related to the Sample Management process and work on new and existing risk analyses. You implement continuous improvement processes within the framework of CAPA measures and participate in Inspection Management. You are part of the First Level Support for your own team and interfaces regarding questions on the Sample Management process.
Independent development and optimization of process flows with a focus on laboratory activities in biotechnology active ingredient production, noting that the position does not include practical laboratory activities.
Independent handling of deviations (Deviations) and CAPAs within the quality management system.
Change Management: Creation and processing of process changes.
Processing, reviewing, and approving documents.
Data Integrity SPOC.
Participation in various squads, possibly leading them.
Participation in internal and external inspections/audits.
Implementation of continuous improvement processes (KVP).
Collaboration on new and existing risk analyses.
Provision of First Level Support for the team and interfaces regarding questions about the Sample Management process.
Completed university degree in a natural or technical field, preferably biotechnology, and at least 5 years of professional experience.
Very good communication skills, fluent in German and good English skills.
Good organizational skills, ability to coordinate projects, and work independently; experience in project management is an advantage.
Knowledge in the pharmaceutical field, GMP, laboratory software applications (LIMS, Unilab), and IT systems; ability to quickly understand and implement complex systems and relationships in practice.
Adaptability to a rapidly changing environment and shifting priorities, as well as interest and experience in analyzing large datasets.
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.