**Job Title-** Quality Assurance Specialist **Location-** Goa **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 coordinator 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, protected 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. + **Languages** : English, Hindi, Konkani, Marathi + **Qualification** :



B.Pharm / M.Pharm + **Experience:** 2-5 Years **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 (https://www.youtube.com/watch?v=SkpDBZ-CJKw&t;=67s) and check out our Diversity Equity and Inclusion actions at sanofi.com (https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness) ! 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 (https://youtu.be/96EwNjb1TLo) 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.

📌 Quality Assurance Specialist (Verna)
🏢 Sanofi Group
📍 Verna