28 Sep
|
Aarti Pharmalabs
|
Navi Mumbai
28 Sep
Aarti Pharmalabs
Navi Mumbai
Role & responsibilities
Key Responsibilities:
API Process Development & Optimization:
- Perform feasibility studies, process optimization, and scale-up of API processes. Conduct process verification and identify Critical Process Parameters (CPPs) and Critical Quality Attributes (CQAs).
- Plan lab work, prepare Reference Standards (RS)/Working Standards (WS), and ensure their characterization.
- Initiate the technology transfer process to the pilot plant or production facility.
Regulatory Affairs & Compliance Support:
- Provide timely technical support for regulatory queries, especially those related to DMF preparation.
- Ensure accurate preparation of specification sheets and MSDS for raw materials and intermediates.
- Prepare the Development History Report for regulatory submission and archival. Conduct initial stability studies for developed products.
Cross-Functional Coordination:
- Coordinate with the Regulatory Affairs (RA), Analytical Development Lab (ADL), IPR, and Development Quality Assurance (DQA) teams.
- Manage coordination between officers working in R&D.;
Required Qualifications & Experience:
- Education: M.Sc. (Organic Chemistry) or Ph.D. (Organic Chemistry) Experience: 2 to 8 years of relevant experience
📌 Senior Executive -Global Regulatory Deficiency Centre (Navi Mumbai)
🏢 Aarti Pharmalabs
📍 Navi Mumbai