Founded in 2007, Biophore has established itself as a trusted partner for niche and complex products.
With 4 US FDA and EU approved API manufacturing facilities, one dedicated intermediate facility and a world class R&D lab housing 400 scientists with varied expertise, Biophore has emerged as one of the leading API companies globally.
We have consistently been in the Top 10 US DMF filers with the US FDA over the past 5 years and with most of our APIs, we are one of the fastest companies to bring them to the market enabling wider access for patients worldwide
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Work Location: Hyderabad
JOB DETAILS:
- Department: Formulation AR&D
- Experience: 2 – 6 Years
- Qualification: B. Pharm /M. Pharm or M Sc
Job Description
1) Method Development and routine analysis of Assay, Dissolution, Related substances, Content Uniformity, Blend Uniformity.
2) Responsible for Analytical Method Validation activities for solid orals and injectables.
3) Responsible for Routine and Stability analysis activities for solid orals and injectables.
4)Responsible for the Review of documents generated in Method development activity.
5)Responsible for the Preparation and Review of Tentative method of analysis and Method development Reports.
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