Role & responsibilities :
Lead end-to-end quality processes for new product/SKU launches, from specifications to commercial release.
Audit and assess contract manufacturers for GMP, regulatory and quality compliance.
Define and implement quality SOPs, testing protocols, inspection processes and batch-release systems.
Review raw materials, CoAs, pilot batches, in-process checks and finished-product testing.
Manage deviations, OOS results, CAPA, complaints and product recalls.
Ensure compliance with applicable Indian regulations, including BIS, CDSCO and Legal Metrology.
Review product labels, claims, ingredients, packaging and shelf-life requirements.
Establish quality agreements and vendor scorecards for manufacturers.




Build quality systems and train internal teams on SOPs and quality processes.

Who You Are :
10+ years of experience in QA/QC and product testing, preferably in Pharma/FMCG.
B.Tech/M.Tech in Chemical Engineering or B.Pharm/M.Pharm.
Strong knowledge of GMP, GLP, ISO, HACCP/FSSC quality systems.
Experience with contract manufacturers, factory audits and CAPA closure.
Solid understanding of analytical/microbiological testing and NABL labs.
Proven experience in taking products from specification to commercial launch.
Comfortable working in a quick-paced startup workplace with travel to manufacturer sites.

📌 Quality Consultant Gurugram (India)
🏢 Vetic
📍 India