R&d – Pharmaceuticals

4 weeks ago

Ankleshwar, Gujarat, India Basic Pharma Life Science Pvt. Ltd. Full time

Assist in formulation development pilot batches stability studies Draft and organize SOPs STPs BMRs calibration logs and regulatory documents Ensure smooth technology transfer from R D to production Coordinate with Analytical QA QC Regulatory and Plant teams Support QA QC audits ensure GMP GDP adherence and contribute to compliance efforts Present progress reports and assist in project tracking Requirements Bachelor s Master s degree in Pharmacy Pharmaceutics or related science field 1-5 years of relevant experience in R D QA QC or documentation roles Knowledge of GMP GLP GDP standards and regulatory guidelines ICH Instrumentation exposure HPLC GC UV is a plus Excellent documentation analytical and communication skills Desirable Experience with NDDS injectable formulations or regulated-market compliance Prior involvement in patent IPR or technology transfer processes Job Type Full-time Pay 160 000 00 - 200 000 00 per year Work Location In person

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