3 - 8 years
1 - 5 Lacs
Posted:2 hours ago|
Platform:
Work from Office
Full Time
The ideal candidate brings 3- 8 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments.
Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety.
The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Own production execution and shift supervision; ensure line clearance, in-process controls, batch documentation accuracy, equipment readiness, and safe operations per SOPs. Additional info:
Qualification: BE / B.Tech
Experience:
5-8 years in agrochemical/chemical industry Must demonstrate strong ownership, attention to detail, and the ability to work in a fast-paced, inspection-ready environment.
Familiarity with ICH, WHO TRS, ISPE, and data integrity principles is expected; hands-on with spreadsheets/ERP/LIMS is a plus.
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