Quality Assurance Specialist

Sanofi Group; Indiana; On-site; USD 6,300 - 13,000; Full time

Job summary

Sanofi Goa site is seeking a Quality Assurance Specialist to uphold product quality and regulatory compliance across the manufacturing lifecycle.

You will oversee IPQA, batch records, deviations, CAPAs, change controls, and QMS coordination while supporting audits and data integrity, ensuring adherence to cGMP and global standards.

Qualifications

• Experience in IPQA, Batch Record Review, and Shopfloor Quality Governance.
• 2 to 5 years of relevant QA experience in pharma manufacturing.
• B.Pharm or M.Pharm with English, Hindi, Konkani, Marathi language skills.

Responsibilities

• Manage Quality Systems compilation, review and PMS for product quality reviews.
• Act as site coordinator for change controls and management of change.
• Oversee Deviation, Market complaint investigation, and CAPA systems.
• Lead training systems and ensure data integrity across QMS.
• Coordinate ICHQ3D, cGMP training, and GMP document control.
• Approve Master/Batch records and lead line clearance and in‑process checks.

Skills

IPQA

Batch Record Review

Shopfloor Quality Governance

Education

B.Pharm / M.Pharm

Job description

Job Title: Quality Assurance Specialist

Location: Goa Site, Verna Industrial Estate, Salcete, Goa, India

About the job

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life‑changing treatments reach people everywhere, faster.

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

• Management of Quality Systems Compilation, Review & Management of overall Product Quality Reviews system.
• Act as site coordinator for change controls & management of change control system.
• Management of Deviation system.
• Management of Market complaint investigation system.
• Act as QA focal point for OOS/OOT management.
• Management of Training system.
• Oversight on Pest Control system.
• To perform Nitrosamine Assessment & review.
• Management of ICHQ3D requirements.
• Site coordinaator for Implementation of Sanofi Global Standards (STDs) and Global Operating Procedures (GOPs)
• Act as focal point for Subcontractors/ Service Providers management.
• Management of overall Validation systems (Process, cleaning, transport & computerized system)
• Management of CAPA System.
• Quality Management Systems Coordinating for conducting self‑inspection as per planner and associated self‑inspection activities.
• Review and Approval of GxP documents, batch manufacturing record and batch packing record in electronic‑document system.
• Implementation of quality documents, management, and control of documents, such as SOPs, Master Documents etc.
• Coordination of cGMP training activity including training of the people & review of training module.
• Initiation, implementation, and closure of change controls.
• Initiation of deviation and support in deviation investigation.
• Support in Market Complaint investigation.
• Implementation of assigned CAPAs and support in closure.
• Implementation of assigned Efficiency Reviews (ERs).
• Act as PPO (Primary Process Owner) for QMI (Quality Maturity Index) as assigned.
• Batch release & response to queries from QP.
• Management of Data integrity aspects.
• Participation and support in SMS initiatives.
• Support for HSE activities.
• Handling of Site Master File (SMF).
• Calibration document review of Engineering/QC/PMTD.
• User access management & review Analytical method creation.
• Audit trail review.
• Document archival/retrieval management.
• Validation & Qualifications Quality focal point for all validations [Process, cleaning, transport & computerized system] and qualification activities.
• Quality focal point for temperature/ relative humidity mapping activities.
• Quality focal point for study related to hold time of products, cleaned/uncleaned equipment hold time, campaign length.
• Quality focal point for utilities & purified water system.
• Management of Site Qualification & Validation Master Plan.
• In‑Process Quality Assurance [IPQA] Review & Approval of Master Batch Records & executed Batch Records Review and Approval of logbooks.
• Line clearance in Production.
• To perform In‑process checks in Production.
• Sampling of products during routine production and validation.
• Quality oversight on shopfloor.
• HSE Adherence to all health safety & environmental aspects as required by company policies and procedures.
• Ensure that the implementation of HSE systems, safe working conditions and maintain a culture of continuous improvement.
• Conducting daily training in the +QDCI meeting address any unsafe condition.
• Take suggestion from associates to improve the work conditions with great safety and zero risk.
• Periodic review of the implemented procedures and evaluation of the same.
• Train people on safety and their job to ensure zero LTI and IWLT at workplace.

About you

• Experience: 2 to 5 Years.
• Technical skills: Experience in IPQA, Batch Record Review, and Shopfloor Quality Governance.
• Qualification: B.Pharm / M.Pharm Languages: English, Hindi, Konkani, Marathi

3 Shift Working

3 Shift Working

Why choose us?

Shape the future of medicine and vaccine delivery with cutting‑edge technology, ensuring seamless launches and a resilient global supply.

Power industry‑leading performance by leveraging digital, data, and AI‑driven innovation at speed and scale.

Transform lives worldwide by delivering life‑changing treatments anywhere, anytime.

Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride.

Work with AI, robotics, and next‑gen automation to redefine global manufacturing and supply.

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!

We are an R&D driven, AI‑powered biopharma company committed to improving people’s lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people’s lives.

We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.

Discover more about us visiting www.sanofi.com or via our movie. We are Sanofi. Start a career that makes a difference.

Reinvention is in our DNA. It’s what drove our evolution from a small French enterprise to one of the world’s leading biopharma companies.

Whether it’s using AI to shorten drug‑discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities. This is where you grow your career.

We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people’s lives.