SH
Pithampur, Madhya Pradesh, India· Full-time
₹6L – ₹7L/yr
SH
Active9mo ago
L 5 - Stability Testing/Analytical Method Development/Process Validation
Role overview
Job description
The Assistant / Deputy Manager – QC will oversee the Quality Control operations at the plant, ensuring compliance with cGMP, regulatory guidelines, and internal quality standards. The role requires strong leadership to manage the laboratory team, maintain robust analytical practices, and support timely release of products. Key Responsibilities Supervise and manage daily Quality Control activities for raw materials, packaging materials, intermediates, and finished products. Ensure adherence to GLP, cGMP, and regulatory requirements (e.g., USFDA, WHO-GMP, EU, etc.). Review and approve analytical data, specifications, and COAs. Oversee method validation, method transfer, and stability studies as per protocols. Investigate out-of-specification (OOS) and out-of-trend (OOT) results and implement corrective and preventive actions (CAPA). Coordinate with cross-functional teams for timely release
…About this listing
- Source: SAVA HEALTHCARE's official careers site (via Keka) · last confirmed on the source 27 Oct 2026
- Posted 22 Jan 2026
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What they are looking for
Skills & requirements
Qualification
8–12 years of experience in Quality Control in the pharmaceutical industry
Department · Quality Control - (Indore)
Hiring company
SAVA HEALTHCARE
Healthcare
View the company profile, current openings and hiring details.
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