AI Overviewதமிழ்A Medical Device Production Supervisor oversees manufacturing teams, ensuring compliance with strict regulatory standards (FDA, ISO 13485) and cGMP. They manage production schedules, optimize workflows, monitor quality control, and lead training to achieve safety and efficiency targets. Key tasks include managing assembly, sterilization, and equipment maintenance. www.glassdoor.co.in +5Key Responsibilities
- Compliance & Quality: Ensure all operations strictly follow GMP (Good Manufacturing Practice), ISO 13485, and company SOPs.
- Production Management: Execute production plans, ensuring efficiency, proper material handling, and adherence to timelines.
- Team Leadership: Supervise, train, and manage the performance of production operators.
- Process Improvement: Identify and implement improvements in manufacturing, such as lean manufacturing principles.
- Documentation: Review production records, logbooks, and investigate quality issues (RCA/CAPA). www.glassdoor.co.in +7
Required Qualifications & Skills
- Education: Typically a Bachelor’s degree in Engineering, Pharmacy, Science, or a Diploma in a relevant field.
- Experience: 1–5+ years in medical device, pharmaceutical, or similar regulated manufacturing.
- Technical Knowledge: Familiarity with ISO 13485, FDA regulations, and cleanroom protocols.
- Skills: Strong communication, leadership, and troubleshooting abilities. www.glassdoor.co.in +5
Typical Reporting Lines
- Reports to: Production Manager or Manufacturing Manager.
- Subordinates: Production Operators, Technicians, Assemblers.
Job Type: Full-time
Pay: ₹25,000.00 - ₹35,000.00 per month
Work Location: In person
