202607-119009 Process Technician (temporary, 2 years)
- Employment type
- Contract
- Location
- Basel
- First posted
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.The PositionAt our location in Basel we offer an exciting position as a shift worker in an innovative and state-of-the-art production environment. In the Basel Drug Substance area, we are responsible for the manufacture of life-saving active ingredients for cancer therapy in our highly automated production facilities for Single Use Technology (SUT) as well as Antibody-Drug Conjugates (ADC).Our demanding manufacturing processes are carried out in strict compliance with Current Good Manufacturing Practices (cGMP) and combine cutting-edge technologies with the highest quality standards. The field of activity includes the production of culture media and buffers, the performance of cell cultures, the purification of biological active ingredients, as well as the manufacture and processing of ADC products in a highly regulated production environment.As an operator, you work across operations within the SUT and ADC operations and actively contribute to providing innovative therapies for patients. In doing so, you operate and monitor highly automated systems, ensure compliance with quality and safety requirements, and work in a dynamic, interdisciplinary team.The opportunity:Execution of biotechnological production processes (Upstream, Downstream, ADC) in compliance with GMP specificationsManufacture and management of media, buffers, samples, as well as consumables and single-use materialsOperation, monitoring, and maintenance of systems including malfunction and alarm managementEnsuring GMP-compliant documentation as well as document control and completionMonitoring the qualified status of systems and supporting material managementRecording, documentation, and reporting of deviations and special occurrencesTraining of employees as well as ensuring safety, order, and cleanliness in the work areaWho are you:Completed vocational training as a chemical and pharmaceutical technologist or comparable trainingSound GMP understanding, ideally with experience in pharmaceutical production or biotechnologyGood knowledge of MS Office (Word, Excel) and ideally in Veeva and MESExperience in handling automated systems on a production scaleVery good German skills in speaking and writing; English skills are an advantageWillingness to work shiftsReady for the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity! Who we areA 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.
Automatically translated from the original.
Posted 2 weeks ago