Roles & Responsibilities:
• Perform routine and advanced quality control analysis of raw materials, in-process samples, and finished products.
• Conduct stability studies in accordance with ICH guidelines.
• Ensure strict compliance with GLP, GMP, and data integrity requirements.
• Maintain accurate analytical documentation, laboratory records, and reports.
• Support internal and external regulatory audits and inspections.
• Operate and handle QC laboratory instruments and analytical techniques.
Qualification:
• B.Sc / M.Sc / B.Pharm / M.Pharm
Experience:
• 1–3 years of Quality Control experience in a regulated pharmaceutical industry.
Skills:
• Hands-on exposure to QC analysis and stability testing.
• Strong understanding of GLP practices and GMP compliance.
• Knowledge of regulatory guidelines (USFDA / WHO-GMP preferred).
• Good documentation and data integrity awareness.
• Ability to work in a regulated, audit-driven environment.
About the Organisation:
Emcure Pharmaceuticals Ltd. is a leading Indian pharmaceutical company with a strong presence in regulated markets, known for its focus on quality, compliance, and innovation, offering stable career growth and exposure to global regulatory standards. Email your application to:
bhavik.parekh@emcure.com
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