About the Role

We are looking for a qualified and detail-oriented Senior Officer (GLP) to ensure compliance with Good Laboratory Practices (GLP) in pharmaceutical laboratory operations. The candidate will be responsible for maintaining laboratory quality standards, monitoring testing activities, managing documentation, and ensuring accurate and reliable analytical results in accordance with regulatory requirements.




Key Responsibilities

  • Ensure implementation and compliance with GLP guidelines.
  • Monitor laboratory activities and analytical testing procedures.
  • Prepare, review, and maintain laboratory SOPs and documentation.
  • Maintain equipment calibration, qualification, and maintenance records.
  • Monitor laboratory investigations, deviations, and CAPA.
  • Coordinate internal audits and regulatory inspections.
  • Ensure proper handling, storage, and traceability of samples.
  • Maintain laboratory records and data integrity.


Requirements

  • Education: B.Pharma, M.Pharma, B.Sc., or M.Sc. in Chemistry, Microbiology, Biochemistry, or a relevant scientific discipline.
  • Male candidates required.
  • Relevant experience in pharmaceutical QC/QA or laboratory operations.
  • Strong knowledge of GLP, GMP, SOPs, and regulatory guidelines.
  • Experience in laboratory documentation, audits, and quality compliance.
  • Good analytical, communication, and problem-solving skills.
  • Knowledge of laboratory instruments and data integrity requirements.


What We Offer

  • Competitive salary based on qualifications and experience.
  • Performance-based incentives, where applicable.
  • Career growth and advancement opportunities.
  • Professional training and technical development.
  • Exposure to pharmaceutical laboratory quality systems and regulatory standards.


Company
KDRS Group
Vacancies
1 Opening
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