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.
At the Basel site, the Pharma Technical Development Synthetic Molecules (PTDC) department is responsible for the technical development of the Synthetic Molecules Pipeline of Drug Substances (DS) and Drug Products (DP) for clinical studies.
The Operations Support & Compliance (OSC) department is responsible for supporting all GMP and non-GMP relevant activities and enabling the development of synthetic and large molecules through high-quality support of our partners. The Laboratory Support and Compliance area focuses on providing reliable support to analytical laboratories and working with many internal and external partners.
You will design and manage master data in SAP S/4HANA for laboratory equipment used in modern analytical laboratories (DS & DP).
You will act as SME (Subject Matter Expert) for the assigned laboratory equipment and organize qualification, regular maintenance, and troubleshooting.
You will connect systems and interfaces and help to optimally interconnect existing and new solutions.
You will work closely with PTD teams in Basel and successfully bring new processes and working methods into everyday life.
You will write and update SOPs, harmonize processes, and ensure that documentation is always GMP compliant.
You will handle changes, deviations, and CAPAs and ensure stable, GMP compliant processes.
You will connect with global stakeholders, promote knowledge sharing, and contribute to projects and initiatives, including continuous improvements.
You have a completed scientific degree (preferably Bachelor or Master) with at least 3-5 years of professional experience or an equivalent qualification through relevant experience in the pharmaceutical industry in a GMP environment of an analytical laboratory or QC.
You work very carefully, structured, and quality-conscious.
You have a strong affinity for systems, databases, and digitalization and experience in managing master data for laboratory equipment in SAP S/4HANA.
You have a strong understanding of GMP, data integrity, and ALCOA+.
You are flexible, work independently, learn continuously, and can set priorities; also in a demanding and dynamic environment.
You are a team player with very good communication skills and enjoy working with local and global stakeholders.
You have fluent German and English skills.
Ready for the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity!
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.
Tagged as: Life Sciences
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