Pharma PDR Formulation RA Job Opening @ Jubilant
Pharma PDR Formulation RA. Research Job. Application is invited along with complete bio-data for the one post of RA PDR Formulation Research project. Interested and Eligible candidates may apply Online. Check out all the details on Rasayanika.com
The manufacturing location at Nanjangud spread on 69 acres is engaged in manufacturing of APIs and caters to the sales worldwide. API portfolio is focused on Lifestyle driven Therapeutic Areas (CVS, CNS) and also targets complex and newly approved molecules. The company is a market leader in four APIs and is amongst the top 3 players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand with 5 acres of infrastructure is USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA audited and approved. This business focusses on B2B model for EU, Canada and emerging markets. It has capabilities to develop multiple dosage forms including Oral solid, injectable and ophthalmic dosage forms. Revenue of the company during the Financial Year 2016-17 was 10,726.09 Million as compared to 9,197.82 Million during the Financial Year 2015-16.
Job Title:Â Research Associate- PDR Formulation
Location: Noida
No.of posts: 01
Qualification – M.Pharmacy Pharmaceutics.
Exp– 2-4 Yrs in a Regulated Market.
Job Description.
- Should have in-depth knowledge of all the equipment of granulation, compression, coating, Wurster process and encapsulation. Should know the concept of scaling up the process from R and D to Pilot Plant to commercial level.
- Should be able to anticipate the problem during the development of formulation with respect to process and product attributes
- Able to work in coordination with development scientist in R and D and PDL scientists at Plant.
- Should know the Regulatory Requirements with respect to documentation, process and product attributes
- Should know the process of alternate vendor evaluation of API and Excipients.
- To execute the R and D trials for troubleshooting/ remediation/ tweaking of commercial products.
- Must have exp in Solid Oral, IR/ER, Pellets based formulation, Liquid Suspension for Regulated Market
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