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Qualification & Data integrity Officer

Sanofi

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33 open qualification roles across 19 companies are on ApplySarthi right now, most of them in Bengaluru (2), Hyderabad (1).

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Counted across 14 company job boards, updated as roles open and close.

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  1. Why do you want to join Sanofi?
  2. What is a weakness you are working on, and how?
  3. Tell me about yourself, and why this role is the right next step.
  4. Tell me about a problem you solved at work that you are proud of.
  5. Tell me about a time you disagreed with your manager. What happened?

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About the job As Quality Assurance Specialist within our Quality team, you'll make sure our daily operations meet Good Practice (GxP) regulations and Sanofi's internal standards. You'll lead the site's Data Integrity program and oversee the qualification and validation of our equipment and systems, so they stay compliant and fit for their intended use. Your work protects product quality and, ultimately, the patients who rely on our medicines. Ready to get started? About Sanofi: We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives. Main responsibilities Lead the site's Data Integrity program: manage the Data Integrity master plan and keep the program running across the site. Build data integrity awareness: train all staff on data integrity requirements and follow up on the training of operators and technicians in all areas. Drive ALCOA+ practices: work with the data integrity governance team to implement ALCOA+ principles (data that is attributable, legible, contemporaneous, original, accurate, and more) in all areas. Plan and review validation activities: confirm the planning and review of activities such as Computer System Validation (CSV), so that systems are fit for their intended use and meet quality standards. Review and approve qualification documents: review and approve qualification protocols and internal documentation for equipment and systems. Monitor and improve validated systems: monitor validated systems on an ongoing basis and put improvements in place to maintain compliance and efficiency. Champion health, safety and environment (HSE): make sure SOPs and changes that need HSE precautions receive HSE approval, follow laboratory safety procedures and PPE requirements, segregate hazardous substances and waste correctly, and report any accidents or incidents to the HSE department. About you Education: Bachelor's degree in Pharmacy or a science discipline. Experience: 3–5 years in similar roles. Technical skills: Knowledge of GxP, computer system validation, equipment qualification and data integrity principles (ALCOA+). Soft skills: Strong communication and training skills, a collaborative mindset, and attention to detail. Safety and ethics: Commitment to HSE requirements, Sanofi's values, code of ethics and personal data protection. Pursue progress , discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !

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Listed on workday · posted 2026-10-21. ApplySarthi collects openings and links to application pages; the role is advertised by Sanofi, not by us.