Job Description

Bei Roche kannst du ganz du selbst sein und wirst fur deine einzigartigen Qualitaten geschatzt. Unsere Kultur fordert personlichen Ausdruck, offenen Dialog und echte Verbindungen. Hier wirst du fur das, was du bist, wertgeschatzt, akzeptiert und respektiert. Dies schafft ein Umfeld, in dem du sowohl personlich als auch beruflich wachsen kannst. Gemeinsam wollen wir Krankheiten vorbeugen, stoppen und heilen und sicherstellen, dass jeder Zugang zur Gesundheitsversorgung hat - heute und in Zukunft. Werde Teil von Roche, wo jede Stimme zahlt.


Die Position
As an integral part of the local Quality Unit, the QA Facility & Engineering team is dedicated to ensuring the qualified state of production facilities for the commercial manufacturing of drug substance materials at Roche in Basel. This team provides quality oversight for the cGMP-compliance status of all production equipment, automation systems, laboratory equipment, building infrastructure, utilities, and IT/OT systems across four critical production areas: large-scale monoclonal antibody production, medium-scale single-use technology for monoclonal antibody production, antibody-drug conjugate production, and synthetic molecule-based active substance production.


This vital role, QA Manager for IT/OT Systems, provides end-to-end quality oversight on the GMP-compliance status of both new and existing IT/OT systems within your assigned area of responsibility, with a specific focus on Manufacturing Execution Systems (MES). You will serve as the crucial QA partner, ensuring system integrity and regulatory adherence across diverse manufacturing and lab environments.

The Opportunity

Provide Quality Oversight: Have end-to-end quality oversight on the GMP-compliance status of new and existing IT/OT systems, especially MES, within your assigned area of responsibility. Assure GMP-Compliance: Proactively provide QA input to assure GMP-compliance in projects and all system lifecycle activities. Act as QA Partner: Serve as the QA-partner for various functions related to key systems, including legacy MES (Simatic IT), future MES (Rockwell Pharmasuite), sLims (LabWare7), SAP S/4HANA, and various embedded systems in production and labs. Perform Review and Approval: Act as the QA reviewer and QA approver of GMP-records in the areas of Technical Change Control, Deviation Management, and CAPAs, as well as CSV deliverables and Standard Operating Procedures (SOPs). Coordinate Investigations: Coordinate and facilitate complex deviation investigations, root cause analyses, and technical risk assessments. Manage Audits/Inspections: Present complex topics during health authority inspections and internal audits alongside partners from various functions. Mentor and Remediate: Mentor technical experts in their inspection preparation and presentation skills, and orchestrate finding remediation if required.

Who You Are

Education and Experience: University degree in life science or engineering and a minimum of 5 years of experience in Quality Assurance at a biologics manufacturing site. System and Process Expertise: Practical experience in Quality Oversight for major IT/OT systems and practical experience in Technical Change Control, Deviation Management, and CAPAs. Communication & Collaboration: Outstanding communication skills and mastery of teamwork in a diverse environment (QA, Production, QC, IT, Engineering, Validation/Qualification) to drive collaboration with partners. Regulatory Acumen: Strong acumen across relevant GMP regulations (e.g., revised Annex 11, GAMP5, etc.), enabling you to drive quality awareness by integrating regulatory requirements, analytical problem-solving, and scientific rationale. Language Skills: Excellent German and English language skills, both written and spoken.

Highly Desirable Experience: Any additional special experience and expertise is highly desirable (e.g., green field / brown field CAPEX projects, implementation of new production or automation technologies, (matrix) people leadership, moderation of authority inspections, PQS implementation projects, etc.).


Ready for the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity!


Wer wir sind
Eine gesundere Zukunft treibt uns zur Innovation an. Mehr als 100.000 Mitarbeiter weltweit arbeiten gemeinsam daran, wissenschaftliche Fortschritte zu erzielen und sicherzustellen, dass jeder Zugang zur Gesundheitsversorgung hat - heute und fur zukunftige Generationen. Durch unser Engagement werden uber 26 Millionen Menschen mit unseren Medikamenten behandelt und mehr als 30 Milliarden Tests mit unseren Diagnostik-Produkten durchgefuhrt. Wir ermutigen uns gegenseitig, neue Moglichkeiten zu erkunden, Kreativitat zu fordern und hohe Ziele zu setzen, um lebensverandernde Gesundheitslosungen zu liefern.


Gemeinsam konnen wir eine gesundere Zukunft gestalten.

Roche ist ein Arbeitgeber, der die Chancengleichheit fordert.