Role & responsibilities
Production Planning & Execution: Execute daily OSD (Oral Solid Dosage - Tablets/Capsules) manufacturing schedules while ensuring full compliance with cGMP standards and safety guidelines.
Batch Manufacturing: Supervise and operate key equipment across dispensing, granulating, compression, coating, and capsule filling operations.
Standard Operating Procedures (SOPs): Adhere strictly to batch manufacturing records (BMRs), standard operating procedures, and safety protocols throughout the manufacturing lifecycle.
Equipment & Room Cleanliness: Oversee line clearance, equipment cleaning, area sanitation, and maintenance of environmental conditions (temperature, humidity, differential pressure).
Yield & Waste Optimization: Monitor process yields, perform end-of-batch material reconciliations, and minimize batch rejections or scrap generation.
Batch Record Documentation: Contemporaneously document all online processing entries,



logbooks, cleaning registers, and process parameters without delays.
In-Process Quality Checks: Perform real-time quality checks including weight variation, hardness, friability, disintegration time, and thickness during compression and coating.
Deviation & CAPA Support: Report shop-floor deviations, non-conformances, and equipment breakdowns immediately, assisting in root cause analysis and implementing CAPAs.
Cross-Functional Coordination: Collaborate closely with Quality Assurance (QA), Quality Control (QC), Warehouse, and Engineering teams to ensure seamless continuous production.
Audit Readiness & EHS: Maintain continuous audit readiness for international regulatory inspections (FDA, MHRA, WHO) and strictly follow EHS guidelines.

📌 Executive Osd Manufacturing Vadodara
🏢 USV
📍 Vadodara