About the Role

We are looking for a detail-oriented QA-IPQA professional to monitor and ensure quality compliance in injection and tablet manufacturing, including dispensing operations. The candidate will be responsible for conducting in-process quality checks, verifying manufacturing activities, maintaining batch documentation, and ensuring adherence to GMP, SOPs, and pharmaceutical quality standards throughout the production process.

Key Responsibilities

  • Perform IPQA activities during injection and tablet manufacturing.
  • Monitor raw material dispensing, weighing, and verification activities.
  • Conduct in-process checks during manufacturing and packaging.
  • Verify batch manufacturing records and dispensing records.
  • Ensure compliance with GMP, SOPs, hygiene, and safety standards.


Requirements

  • Education: B.Pharma, M.Pharma, B.Sc., or M.Sc. in a relevant scientific discipline.
  • Male candidates required.
  • Relevant experience in pharmaceutical QA/IPQA preferred.
  • Knowledge of injection and tablet manufacturing processes.
  • Understanding of dispensing, documentation, GMP, and quality procedures.


What We Offer

  • Competitive salary based on qualifications and experience.
  • Performance-based incentives, where applicable.
  • Career growth opportunities in Quality Assurance.
  • Professional training and skill development.
  • Exposure to pharmaceutical manufacturing and quality operations.


Company
KDRS Group
Vacancies
4 Openings
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