1 - 5 years

1 - 2 Lacs

Posted:9 hours ago| Platform: GlassDoor logo

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Work Mode

On-site

Job Type

Full Time

Job Description

  • 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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