M Pharma Research Associate jobs @ Jubilant Life Science
M Pharma Research Associate jobs @ Jubilant Life Science. Career @Â Jubilant Life Science. Pharmacy jobs. M Pharmacy jobs. Check out all the details on the same below:
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 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: Research Associate
Location:Â Â R&D Centre-II, IND
Function:Research & Development
Qualification– M,Pharmacy
Experience: 0-2 Years
Job description:
- Support entire drug product development process starting with first pre-formulation studies up to the manufacturing process transfer to production and the provision of the required documentation to allow worldwide registration
- Support the development of robust formulations and processes through optimization, scale-up and validation work applying QbD principles incl. risk assessments and DoEs
- Provide documentation of raw data, evaluation and contribute to the interpretation of results. Provide input for the selection of next experiments.
- Communicate and address problems, perform safety and literature searches under guidance from more experienced team members.
- Preparation and planning of all activities related to product development and tech transfer
- Review of all documents to support regulatory filings to various markets
- Must have understanding about the development of Parenteral formulations, Injectable dosage forms
