Production Executive OSD
2 days ago
- The ideal candidate brings 5 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:
- Bachelors degree in relevant field (B.E / B.Tech / B.Sc / M.Sc)
- 3 to 8 years of relevant industry experience
- Good interpersonal and communication skills
- Willingness to relocate
- API Pharmaceutical Industry experience preferred
- 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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