R&d - Pharmaceuticals

2 days ago

Ankleshwar, 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.

Pay: ₹160,000.00 - ₹200,000.00 per year

Work Location: In person

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