Executive - OSD Manufacturing

USV; Poicha; On-site; INR 600,000 - 900,000; Full time

Job summary

USV is seeking a Production Planner/Operator to manage daily OSD manufacturing schedules while ensuring adherence to cGMP and safety standards. You will supervise core equipment across dispensing, granulating, compression, coating and capsule filling, and maintain strict documentation and batch records.

The role requires tight cross-functional coordination with QA, QC, warehouse and engineering to sustain continuous production and audit readiness for international inspections.

Responsibilities

• Execute daily OSD (Oral Solid Dosage - Tablets/Capsules) manufacturing schedules while ensuring full compliance with cGMP standards and safety guidelines.
• Supervise and operate key equipment across dispensing, granulating, compression, coating, and capsule filling operations.
• Adhere strictly to batch manufacturing records (BMRs), standard operating procedures, and safety protocols throughout the manufacturing lifecycle.
• Oversee line clearance, equipment cleaning, area sanitation, and maintenance of environmental conditions (temperature, humidity, differential pressure).
• Monitor process yields, perform end-of-batch material reconciliations, and minimize batch rejections or scrap generation.
• Contemporaneously document all online processing entries, logbooks, cleaning registers, and process parameters without delays.
• Perform real-time quality checks including weight variation, hardness, friability, disintegration time, and thickness during compression and coating.
• Report shop-floor deviations, non-conformances, and equipment breakdowns immediately, assisting in root cause analysis and implementing CAPAs.
• Collaborate closely with Quality Assurance (QA), Quality Control (QC), Warehouse, and Engineering teams to ensure seamless continuous production.
• Maintain continuous audit readiness for international regulatory inspections (FDA, MHRA, WHO) and strictly follow EHS guidelines.

Job description

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.