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 Position

Job Summary

• Overarch the site-level validation framework and define technical strategies for Process Validation (PV), Cleaning Validation (CV), and Test Method Validation (TMV).

• Drive competence development within MSAT regarding validation methodologies, statistical tools, and standardized systems, demonstrating in-depth mastery of IVD reagent manufacturing processes (bulk compounding, formulation, lyophilization/freeze-drying, filling, etc.).

• Provide authoritative technical consulting, risk rationales, and deep-dive troubleshooting for complex PV, CV, and TMV topics across the site.

• Serve as the core Subject Matter Expert (SME) during internal and regulatory audits (e.g., NMPA, FDA, ISO).

• Foster validation excellence and operational efficiency through Lean/Agile methodologies, statistical rigor, and digitalization tools.

• Ensure ‘Right to Operate’ through full compliance with all applicable GMP, SHE, and other global and local regulatory requirements, as well as Roche Quality and SHE policies and standards.

Main Tasks & Responsibilities

• Overarch and optimize site-level validation strategy documents; establish and maintain comprehensive Validation Master Plans (VMP) covering Process, Cleaning, and Test Method Validation.
  
• Establish technical standards, validation rationales (e.g., family, matrixing, bracketing, worst-case evaluation criteria), and define lifecycle validation strategies .
  
• Proficiently apply statistical tools to design, establish, and deploy scientifically sound sampling strategies.
  
• Act as the senior validation technical interface connecting the site with global technical networks, ensuring dynamic scientific alignment and technical support.
  
• Deliver high-level validation impact assessments, technical feasibility studies, and robust validation strategies for critical manufacturing changes (e.g., raw material localization/source changes, recipe sequence adjustments).
  
• Lead root cause analyses and in-depth technical investigations for validation non-conformances, driving effective corrective and preventive actions.

• Drive validation technical competence within MSAT; establish and standardize protocols, report templates, and sound scientific rationale frameworks across PV, CV, and TMV domains.
  
• Lead or champion Continuous Improvement (CI) and Lean initiatives to eliminate process waste, streamline validation strategy, and enhance site operational performance.
  
• Provide strategic validation support during new technology introductions and cross-site technical transfers, ensuring seamless cross-functional handover and flawless project delivery.
  
• Ensure ‘Right to Operate’ through compliance with all global and local regulatory requirements applicable to RDSZ

• Implement and apply the RDSZ Quality Management System (QMS)

• Ensure all applicable SHE requirements been fulfilled to comply with corporate group policy and local regulations
  

Qualifications

• Bachelor Degree in Pharmaceutical Engineering, Chemistry or Biology or equivalency. Preferred: Master Degree in Pharmaceutical Engineering, Chemistry or Biology or equivalency
• Good command of written and spoken English
• Above 6 years’ experience in a highly regulated cGMP manufacturing environment or equivalency
• Related work experience in the Diagnostics, Pharmaceutical, Medical device Industry as Q&V engineer or expert.
• Solid understanding of the QC/QM/Regulatory process
• Reagent or liquid solution manufacturing process development experience.
• Strong team oriented
• High level attention to detail and strong analytical skills 
• Flexible and able to prioritize own work
• Ability to work across functions within the organization/project
• A “can-do” attitude and willingness to go the extra mile when required
• Intercultural understanding and ability to work effectively with other nationalities
• Achieving Results
• Strong technical acumen
• Strong communication and coordination skills 
• Strong continuous improvement expertise
• Superior problem-solving skills with proven ability to anticipate issues and recommend effective and efficient solutions

Who we are

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.