Job Description


  • Execute and monitor the production of Oral Solid Dosage (OSD) formulations in accordance with approved SOPs and batch records.
  • Ensure compliance with GMP, safety, and quality standards throughout all stages of production.
  • Collaborate with cross-functional teams to support smooth workflow and resolve production-related issues.
  • Maintain accurate and timely documentation of all production activities.
  • Participate in shift operations as required, demonstrating flexibility and reliability.
  • Contribute to continuous improvement efforts and process optimization initiatives.



Requirements

  • Qualification:   ITI / Diploma / D.Pharm / B.Sc
  • Experience:   2–6 years in OSD Formulations (mandatory)
  • Candidates from NAPS / NATS / Technical Contract Services with formulation production experience are eligible
  • Willingness to work in shift operations



Apply for this Position

Ready to join ? Click the button below to submit your application.

Submit Application