Title:  QC Analyst

Job Summary:

This position shall be responsible for sample analysis and adherence of cGMP compliance as per Sun Pharma Quality Standards for Quality Control Laboratory at Drug Substance Manufacturing site.

Essential Job Functions:

• Inprocess sample analysis.
• Intermediate sample analysis.
• Finished product sample analysis.
• Raw material sample analysis.
• Packing material analysis.
• Environmental monitoring.
• Instrument calibration.
• Sample registration and entry in LIMS.
• Other activities entrusted from time to time.

Requirements and Qualifications:

A minimum bachelor’s degree in Science is required. A minimum 2years of experience in pharmaceutical quality management system .Good knowledge in cGMP and cGLP of Drug and Cosmetic Act in both domestic and international regulatory environments. Person should have exposure on analysis. Working knowledge of regulatory requirements/ guidelines for various country, latest updates on regulations.

Motivate people with a variety of skill sets is required. Strong organizational, interpersonal and communication skills are essential. Excellent interpersonal skills and ability to communicate effectively with middle management levels of the organization and external stakeholders.