This position is responsible for managing all Quality Control Operations of a WHO-GMP & ISO approved Tablets and Capsule manufacturing facility.
Specific Responsibilities:
• To perform HPLC and Dissolution analysis
• To review and check all Raw material, packing material, bulk and finish product specification, method of analysis and all worksheet.
• To review and check Different validation protocol like process, cleaning, analytical method.
• To review and check Stability study and hold time study protocol
• To ensure for timely sampling and analysis of incoming materials, like raw materials, packing materials
• To ensure for timely analysis of bulk, finish product, stability sample and validation sample.
Qualifications / Requirements:
• Experience of performing HPLC analysis
• Bachelor's degree in a scientific discipline (Masters Preferred).
• 3-7+ years of hands on experience in the pharmaceutical industry, with specific experience in Quality Control
Job Types: Full-time, Permanent
Pay: ?16,000.00 - ?35,000.00 per month
Schedule:
• Day shift
Supplemental pay types:
• Yearly bonus
Work Location: In person
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