Jubilant Pharma Research Scientist Job Opening – Apply Online
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. Check out all the details
Job Title: Research Scientist – Synthesis
LOCATION: R&D Centre – I, IND
COMPANY: Jubilant Generics Limited
FUNCTION: Research & Development
Qualification– M.Pharm( Medicinal Chemistry)
Experience– 2-3 Years
Job Description-
- Identifying the various possible routes of synthesis.
- Collection and compilation of literature of assigned projects
- Completion of process development in stipulated time.
- Designing, verifying and analyzing the research data.
- Reducing the cost of the product through process improvement.
- Transferring the developed technologies at the pilot plant/plant.
- Timely updating of Lab Notebooks as and when the experimentation is completed.
- Responsible for the preparation of technical packages.
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 manufa
cturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively.Job Description:
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 focusses 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 state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses 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.
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