Microbiologist – QC Laboratory (Full‑time)

About the role

Support microbiology for the Cipla Saudi site, ensuring timely execution of QC microbiology laboratory qualifications, validation activities, procurement, and compliance with cGMP, data integrity, and regulatory requirements.

Key responsibilities

• Prepare procurement documents (URS, SIA, PRA & GxP) and qualify new microbiology instruments/equipment.
• Conduct area qualifications, temperature mappings, and equipment calibrations/AMC scheduling.
• Execute QC operations, prepare protocols, reports, and ensure ALCOA++ compliance of raw data and laboratory records.
• Maintain inspection readiness for SFDA, EU GMP, MHRA, WHO, and PIC/S audits and support regulatory audit responses.
• Train analysts and team leaders on HPLC/UPLC, GC, UV, FTIR, dissolution and advanced analytical techniques.

Required profile

• M.Sc. in Microbiology (preferred).
• 8‑10 years of pharmaceutical microbiology experience with strong knowledge of microbiological testing techniques, method validation/verification, method transfer, environmental monitoring, instrument calibrations/validations/qualifications, and stability support.

Required skills

• HPLC
• UPLC
• GC
• UV spectroscopy
• FTIR
• Dissolution testing
• Method validation and transfer
• Microbiological testing techniques
• Environmental monitoring
• Instrument calibration and qualification
• Stability support