About the Role

We are looking for an experienced and result-oriented Quality Head to oversee quality assurance and quality control operations in the pharmaceutical industry. The candidate will be responsible for maintaining product quality, ensuring regulatory compliance, implementing quality management systems, and maintaining GMP standards.

Key Responsibilities

  • Lead and manage Quality Assurance (QA) and Quality Control (QC) departments.
  • Ensure compliance with GMP, GLP, WHO-GMP, and other regulatory guidelines.
  • Monitor manufacturing processes, product quality, and documentation.
  • Review and approve SOPs, batch records, and quality-related documents.
  • Handle audits, inspections, deviations, CAPA, and change control.
  • Ensure proper validation, calibration, and quality management systems.
  • Coordinate with production, R&D, regulatory affairs, and other departments.
  • Maintain continuous improvement in quality standards and processes.


Requirements

  • Educational Qualification: B.Pharma, M.Pharma, B.Sc. or M.Sc. in Chemistry, Microbiology, Biochemistry, or a relevant scientific discipline.
  • Relevant experience in pharmaceutical QA/QC or quality management.
  • Strong knowledge of GMP, GLP, WHO-GMP, and regulatory requirements.
  • Experience in handling audits, inspections, CAPA, deviations, and documentation.
  • Excellent leadership, analytical, communication, and decision-making skills.
  • Ability to manage quality teams and ensure regulatory compliance.
  • Knowledge of pharmaceutical manufacturing processes and quality standards.


What We Offer

  • Competitive salary package based on qualifications and experience.
  • Performance-based incentives.
  • Leadership and career advancement opportunities.
  • Professional development and regulatory training.
  • Opportunity to lead quality operations and implement quality improvement initiatives.
  • Exposure to pharmaceutical manufacturing and regulatory compliance systems


Company
KDRS Group
Vacancies
1 Opening
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