• Conduct analytical testing using HPLC, UV, GC, and related instruments.
• Perform microbiological testing including sterility, endotoxin, microbial limits, and water testing.
• Carry out environmental monitoring of cleanrooms and controlled areas.
• Prepare, analyse, and interpret laboratory samples to support batch release and stability studies.
• Maintain laboratory documentation in compliance with GMP and regulatory standards.
• Participate in investigations, deviations, and out-of-specification (OOS) results.
• Calibrate, validate, and maintain laboratory equipment.
• Support continuous improvement initiatives within the laboratory.

Requirements:

• Degree or Diploma in Chemistry, Microbiology, or related scientific field.
• 2–4 years’ experience as a QC Lab Analyst in the pharmaceutical industry.
• Proven hands-on experience with HPLC analysis.
• Strong background in pharmaceutical microbiology testing and GMP practices.
• Familiarity with GLP, GMP, and regulatory guidelines (e.g., MCC, FDA, or EMA).
• Excellent attention to detail, problem-solving, and documentation skills.

Attributes:

• Strong technical ability and analytical mindset.
• Reliable, accurate, and detail-oriented.
• Ability to work independently and as part of a team.
• Flexible and able to adapt to changing priorities.