Production Supervisor

Production Supervisor Vein360 - 5.0 Blue Ash, OH Job Details Full-time 1 day ago Qualifications Manufacturing management Medical equipment sterilization Operations management 5 years Labeling Safety standards in production Environmental compliance Hazard Communication Standard Improving operational efficiency High school diploma or GED Hiring Supervising experience Continuous improvement Conflict management Quality inspection Cleaning Quality standards in production Training & development Senior level Crew management Overseeing training FDA regulations

Full Job Description Summary of Position:

Production Supervisor works under the supervision of Director of Operations or their designee and is responsible for ensuring the safety, quality and efficiency of daily operations at Vein360. Production Supervisor applies relevant experience, knowledge and skill sets to manage one or more production operators, including time management, training, conflict resolution and review of device history records. The Production Supervisor is to become an expert in each phase of reprocessing operations and able to provide meaningful input to operations leadership and quality assurance for the continuous improvement of these operations.

Essential Functions:

Works within a production environment to ensure the reliable execution of reprocessing operations which include: Receiving used healthcare products Incoming inspection of raw materials Cleaning Drying Inspection & testing Packaging & labeling Sterilization load preparation Device history record review Hiring and training of new production associates, including re-training as appropriate. Strictly adhere to, and enforce compliance with, all corporate environmental health and safety programs. including bloodborne pathogens and hazard communication. Faithfully execute work instructions as required and ensure the same for all assigned production associates. Identify opportunities for improvement and provide feedback to operations and quality. Support quality system initiatives as assigned. Comply with applicable FDA requirements and all associated standards / guidances.

Education:

Minimum:

High school diploma or

GED Experience:

5+ years of supervisory experience within FDA regulated medical device operation

Preferred Skills/Qualifications:

Working knowledge of 21 CFR 820 (Quality System Regulation) with specific experience with: Good Documentation Practice Production & Process Controls Acceptance Activities Training