The Production Supervisor is responsible for supervising day-to-day manufacturing operations, ensuring production targets are achieved in compliance with ISO , GMP, safety, and quality standards. The role involves manpower supervision, process control, coordination with QC/QA, and maintaining documentation and discipline on the shop floor. And Finish goods dispatch.
Key ResponsibilitiesProduction Operations
- Supervise medical device manufacturing processes including packing and dispatching finish goods.
- Ensure production as per approved production plans, SOPs, and work instructions
- Monitor machine performance and minimize downtime/rejection.
Process Control & Quality Compliance
- Ensure adherence to ISO, and GMP requirements on the shop floor
- Monitor critical process parameters (Packing, Foiling)
Manpower Management
- Allocate manpower shift-wise and ensure adequate staffing
- Train operators on SOPs, GMP, safety, and hygiene practices
- Maintain discipline, attendance, and productivity of shop-floor staff
Material & Inventory Control
- Coordinate with stores for availability of raw materials and packaging materials.
- Minimize material wastage and ensure proper material handling
- Maintain production records related to material consumption and dispatch.
Documentation & Reporting
- Maintain Batch Manufacturing Records (BMR), production logs, and shift reports
- Record production output, rejection, rework, and downtime data
- Ensure accurate and timely documentation for audits and traceability
Safety, Hygiene & GMP
- Ensure compliance with safety guidelines, PPE usage, and housekeeping standards
- Maintain hygiene and cleanliness in production and controlled areas
- Support environmental monitoring and pest control activities
Continuous Improvement
- Identify process improvement opportunities to enhance productivity and reduce defects
- Support validation, process optimization, enhance productivity.
Required Qualifications
- Bachelor’s Degree in Science, Polymer Engineering, Rubber Technology, Bachelor in Science, or related field
- Diploma holders with relevant experience may also be considered.
Experience Requirements
- 2–3 years of experience in production or packing supervision in medical device manufacturing, rubber/latex products, medical devices, or pharmaceutical industry
- Experience in regulated manufacturing environments preferred
Skills & Competencies
- Strong knowledge of condom manufacturing processes and latex technology
- Understanding of ISO and GMP requirements
- Leadership and team-handling skills
- Problem-solving and decision-making ability
- Ability to work in shifts and factory environments
- Basic computer skills (MS Office, ERP systems)
Working Conditions
- Factory-based role
- Rotational shift duties (day/night)
- Strict adherence to GMP, safety, and hygiene protocols
Job Types: Full-time, Permanent
Pay: ₹18,000.00 - ₹22,000.00 per month
Work Location: In person
