Dr. Reddy€™s Laboratories Ltd. (NYSE: RDY) is an integrated global pharmaceutical company, committed to providing affordable and innovative medicines for healthier lives. Through its three businesses – Pharmaceutical Services and Active Ingredients, Global Generics and Proprietary Products €“ Dr. Reddy€™s offers a portfolio of products and services including APIs, custom pharmaceutical services, generics, biosimilars and differentiated formulations. Major therapeutic focus is on gastro-intestinal, cardiovascular, diabetology, oncology, pain management and anti-infective. Major markets include India, USA, Russia-CIS and Europe apart from other select geographies within Emerging Markets. For more information, log on to: www.drreddys.com
Vacancy Details
Roles & Responsibilities
1. Handling of Incident investigations, tracking of incidents, participation and co-ordination with the team for the investigations.
2. Review and monitoring of process and cleaning validations at site and ensure the compliance to regulatory guidelines.
3. Review & Approval of Master documents (BPR/Master formula/Process flow/SOP/Spec & MOAS etc.) of products.
4. Trending of the incidents/ OOS/ OOT and CAPA according to the defined timelines.
5. Incident investigations, tracking of incidents, Review and monitoring of process and cleaning APQR preparation, Handling of Market complaints, Handling of customer / regulatory audits
Interested candidates share their CV at What’s App @ 9491795337 / 9966664639
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