- Conduct data reviews to ensure compliance with GLP (Good Laboratory Practices) regulations.
- Perform HPLC analysis on samples to detect impurities and contaminants.
- Review batch records, stability studies, and other documentation for accuracy and completeness.
- Identify and report any discrepancies or issues found during the review process.
Job Requirements :
- 2-6 years of experience in a pharmaceutical or life sciences industry setting.
- Robust understanding of GLP guidelines and regulations.
- Proficiency in HPLC analysis techniques.
- Ability to conduct thorough data reviews and identify errors or discrepancies.
📌 Quality Control Officer (Paonta Sahib)
🏢 Pontika Aerotech
📍 Paonta Sahib
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.