The role involves supervising a controlled environment room to meet established production schedules while maintaining a productive work environment
Job Summary
The role involves supervising a controlled environment room to meet established production schedules while maintaining a productive work environment.
Candidates must possess a thorough understanding of current Good Manufacturing Practices (cGMPs) and apply them to process operation and control.
This position requires acting as a liaison between manufacturing, R&D, and engineering to ensure engineering requests are processed correctly and timely.
Matching Summary
The role involves supervising a controlled environment room to meet established production schedules while maintaining a productive work environment.
Skills & Requirements
Must-have
High volume manufacturing experience
Medical device industry background
Process validation and transfer knowledge
Current Good Manufacturing Practices (cGMP) expertise
Team training and development capabilities
Production schedule execution and yield management
Nice-to-have
Experience with start-up and scale-up phases
Ability to collaborate with R&D and engineering
Strong problem-solving skills for process issues
Flexibility to work various shifts
Passion for improving human health outcomes
Key Requirements
Bachelor's degree from a four-year college or university
2 to 5 years of related experience in high volume manufacturing