What are the responsibilities and job description for the Production Supervisor position at POLYMEDCO, INC?
The Production Supervisor oversees daily operations within the medical device kitting department, ensuring efficient workflow, compliance with quality standards, and adherence to safety regulations. This role involves supervising production staff, optimizing processes, and ensuring timely fulfillment of customer orders.
Key Responsibilities:
Production & Operations Management:
- Supervise daily kitting operations, ensuring efficiency and accuracy in assembling medical device kits.
- Monitor production schedules, manage workflows, and adjust resources as needed to meet deadlines.
- Ensure compliance with Good Manufacturing Practices (GMP) and FDA regulations.
- Implement and maintain Standard Operating Procedures (SOPs) for kitting operations.
- Coordinate with other departments (Quality, Supply Chain, Customer Service to ensure seamless production.
Quality & Compliance:
- Enforce quality control measures to ensure kits meet regulatory and company standards.
- Identify and resolve quality issues, working closely with Quality Assurance teams.
- Maintain documentation and reports in compliance with FDA, ISO 13485, and other regulatory requirements.
Team Leadership & Development:
- Train, coach, and mentor production staff to ensure high performance and compliance with procedures.
- Conduct performance evaluations and provide feedback for continuous improvement.
- Foster a culture of teamwork, accountability, and continuous improvement.
Safety & Continuous Improvement:
- Ensure a safe working environment by enforcing safety protocols and conducting regular inspections.
- Lead process improvement initiatives to enhance productivity and reduce waste.
- Identify opportunities for automation or efficiency gains in kitting operations.
Qualifications & Requirements:
- Associate or Bachelor’s degree or equivalent experience in a related field preferred.
- 3-5 years with progressing responsibility within a medical device or regulated manufacturing environment.
- Strong leadership and problem-solving skills.
- Advanced computer skills
- Knowledge of FDA, ISO 13485, and GMP regulations.
- Proficiency in ERP/MRP systems and production planning tools.
- Excellent communication and organizational skills.
