Our Client, a well known Pharmaceutical company is looking for an experienced QC Senior Analyst. Reporting to the QC Team Leader your responsibilities will include:
- Perform analyses using industry-standard techniques, including HPLC, GC, Spectrophotometry, Dissolution testing, and Microbiological assays.
- Ensure all testing is conducted in line with established analytical methods, SOPs, and regulatory requirements, with accurate documentation adhering to Good Documentation Practices (GDP).
- Conduct and monitor stability studies to assess product shelf life and performance under various storage conditions.
- Collaborate with cross-functional teams to support investigations, root cause analysis, and the implementation of CAPAs.
- Carry out sampling of raw materials, intermediates, and finished pharmaceutical products following approved procedures.
- Maintain compliance with Good Laboratory Practice (GLP) and Health & Safety protocols to ensure a safe, efficient, and reliable laboratory environment.
Working Hours: Office Hours
Requirements
- Experience in a pharmaceutical QC laboratory, ideally within a GMP-regulated setting.
- Demonstrated proficiency in analytical techniques such as HPLC, GC, Spectroscopy, and/or Microbiological analysis.
- Strong attention to detail, excellent problem-solving skills, and the ability to work effectively under pressure.
- Good command of English, both written and spoken.
Education and Experience
- Degree in Chemistry, Pharmaceutical Sciences, Microbiology, or a related scientific discipline.
Benefits
- Health Insurance
- Annual Performance Bonus
Job Reference: GX706
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