About the Role

We are seeking a qualified and experienced Quality Manager to supervise pharmaceutical quality operations and ensure products meet established quality and safety standards. The role involves maintaining regulatory compliance, strengthening quality systems, and ensuring consistency across manufacturing and testing processes.

Key Responsibilities

  • Monitor and control daily QA/QC activities.
  • Ensure compliance with GMP, GLP, and WHO-GMP standards.
  • Handle quality audits, inspections, and documentation.
  • Manage deviations, CAPA, product complaints, and investigations.
  • Coordinate with production, R&D, and regulatory departments.



Requirements

  • Education: B.Pharma, M.Pharma, B.Sc., or M.Sc. in Chemistry, Microbiology, Biochemistry, or a relevant field.
  • Male candidate required
  • Relevant experience in pharmaceutical QA/QC operations.
  • Strong knowledge of GMP, GLP, and regulatory guidelines.
  • Good analytical, technical, and problem-solving skills.
  • Excellent leadership, communication, and team management abilities.


What We Offer

  • Competitive salary based on qualifications and experience.
  • Performance-based incentives and rewards.
  • Career growth and leadership opportunities.
  • Professional training and skill development.
  • Exposure to pharmaceutical quality systems and regulatory standards.


Company
KDRS Group
Vacancies
1 Opening
Apply Now Create CV ATS Friendly

No charges. KDRS Group never asks candidates for fees.

View All Jobs