Assistant Manager Quality Control, Pharmaceuticals

Job Description:

Responsibilities

• Performing and organizing timely analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals.
• Performing and organizing analysis of market complaints, Stability, process validation, Cleaning Validation samples of Pharmaceuticals.
• Good Laboratory Practice
• Performing and organizing calibration / maintenance of lab. Equipment and assisting for the qualification of laboratory equipment.
• Reviewing pharmacopeias for specification preparation.
• Preparing SOPs, Formats, Specification, Analytical Test Record and other documents.
• Managing reference standards, working standards, Laboratory chemicals & reagents.
• Managing instrument laboratory with reference to spares, maintenance etc.
• Managing Control Samples and related record.
• Approval / Rejection of Raw Materials, Packaging materials, in process materials, Bulk Finished products and bulk medical device.
• Investigating out of specification results, retesting and review the analysis records.
• Maintaining & reviewing laboratory raw data and log book related to testing activity.
• Responsible for reviewing the chromatographic data.

Qualification & Expeirence

• Post Graduate in Science (Organic or Analytical Chemistry) or B.Pharm/M.Pharm
• 5-7 years in chemical & instrumental testing laboratory with exposure to GMP, GLP