Oversee validation and qualification activities related to manufacturing, processes, cleaning, equipment and systems.
Ensure effective handling of market complaints, product quality issues and investigations.
Formulation and process development activities for parenteral pharmaceutical products. Pre-formulation, compatibility, stability and optimization studies.
Completion of designated projects and tasks supporting European Market RA and International Market RA, according to internal Work Instructions, with guidance and direction by the manager and more senior colleagues.
Sun Pharma is India’s No. 1 pharmaceutical company and a leading global player in specialty medicines. With over 40 manufacturing facilities and a diverse portfolio, we deliver high-quality medicines across 100 countries
B. Pharm M. Pharm M.Sc. Chemistry. Chromatographic analysis (HPLC) with Empower 3 software & LI MS Awareness
CMP documentation & data integrity, HPLC Testing of raw materials, in-process & finished products
Testing & Method Validations; Culture Handling, Water & Bioburden Testing; Raw Material and BET Testing Water, Finished and Stability samples, Autoclave, Sterility Testing & observation of canisters.
To support and execute Analytical Method Validation activities, ensure data integrity and regulatory compliance for API products at our Udaipur API Plant.