Executive - OSD Manufacturing

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.