Senior Executive-QC

As a member of Jubilant Pharma Limited, you will be part of a global integrated pharmaceutical company that offers a wide range of products and services to customers across geographies. The company organises its business into two segments: - **Specialty Pharmaceuticals**: This segment includes Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products. - **Generics & APIs**: This segment comprises Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly-owned subsidiary of Jubilant Pharma with Research & Development units in Noida and Mysore, India. JGL operates two manufacturing facilities - one in Mysore, Karnataka, and the other in Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing respectively. The Mysore manufacturing site, spread over 69 acres, is a USFDA approved facility that manufactures APIs targeting Lifestyle driven Therapeutic Areas (CVS, CNS). The Roorkee facility is state-of-the-art and approved by multiple regulatory bodies including USFDA, Japan PMDA, UK MHRA, TGA, WHO, and Brazil ANVISA, focusing on a B2B model for EU, Canada, and emerging markets. At Jubilant Pharma, R&D is a key focus with around 500 professionals based in Noida and Mysore working on developing new products in API, Solid Dosage Formulations (Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams, and Liquids). The company conducts BA/BE studies in-house with global regulatory accreditations. JGL's Regulatory Affairs & IPR professionals ensure a unique portfolio of patents and product filings in regulatory and non-regulatory markets. The company's revenue has shown consistent growth, reaching INR 53,240 Million in the Financial Year 2018-19. In this role, your responsibilities will include: - Incoming QC - Sampling and analysis of packing material/raw material - In Process QC - Preparation of specifications, general test procedures, and standard test procedures - Maintenance of artworks & shade cards - Equipment calibration and validation - Recording of analytical data - Preparation of records of analysis for RM / FP and stability samples - Ensuring cGMP and GLP compliance - Investigation of deviations, incidents, and OOS - Area maintenance to ensure good housekeeping in the lab For more information about the organization, please refer to [www.jubilantpharma.com](www.jubilantpharma.com).,