Job Description
- 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.
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