SR EXECUTIVE-QUALITY CONTROL AT JUBILANT PHARMOVA
DATE POSTED: 28/09/23
COMPANY: Jubilant Pharmova Limited
Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients.
Jubilant Generics (JGL) is a wholly-owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities, one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively.
The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs and caters to the sales worldwide. API portfolio focuses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is a state-of-the-art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focuses on B2B model for EU, Canada, and emerging markets.
Both manufacturing units are backward-integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services.
JGL’s full-fledged Regulatory Affairs & IPR professionals ensures a unique portfolio of patents and product filings in regulatory and non-regulatory market.
Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018-19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18.
Kindly refer www.jubilantpharma.com for more information about organization.
- Should have experience in handling empower application software
- Must have one year of experience in handling as a HPLC analysis
- In-depth knowledge of document practices
- Should know the procedure for lab incident, deviation, and OOS management
- Should adhere to the testing SLA
- Should adhere to the SOPs and policies at all times
- Should adhere to data integrity policy at all times
- Should record all the testing results and log books as per respective SOP
- Should complete training as scheduled
- Should have minimum awareness of regulatory guidelines like ICH Q& and 21 CFR
Qualification and Experience:
Degree in Science/Post Graduate in Science (Chemistry)/ Bachelor of Pharmacy/Master of Pharmacy with 2+ Years of experience in API industry.
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