R&d – Pharmaceuticals

Year    Ankleshwar, GJ, IN, India

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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Job Detail

  • Job Id
    JD4024824
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Ankleshwar, GJ, IN, India
  • Education
    Not mentioned
  • Experience
    Year