KC291
Located in:
Kentwood, MI
Pay: $90,000-$110,000/year, depending on experience
Job Full Description:
A global leader in the manufacturing of orthopedic implants, spinal implants, precision instruments, and orthopedic cutting tools is seeking a Medical Device Production Manager to join its innovative team. Specializing in high-precision CNC milling, turning, and cutter grinding, this organization is committed to delivering exceptional quality and service to its customers. Reporting to the General Manager, the Production Manager will lead continuous improvement efforts and oversee daily production operations to ensure safety, quality, and efficiency.
Medical Device Production Manager Responsibilities:
- Develop and implement continuous improvement plans and facilitate area team meetings to prioritize activities.
- Directly engage with customers to address quality, delivery, and compliance concerns.
- Evaluate team needs, including staffing, tools, and equipment, and remove barriers to productivity.
- Oversee production processes to ensure high-quality output in a safe, efficient manner.
- Provide mentorship and leadership to Team Leaders, fostering growth and development.
- Collaborate with other managers to align production goals with overall company objectives.
- Coordinate with cross-functional teams in areas such as quality assurance, engineering, and maintenance.
- Identify opportunities for improvement using data-driven problem-solving tools.
- Ensure team members receive appropriate training, development, and performance reviews.
- Lead project start-up teams and oversee the implementation of production systems.
- Maintain compliance with FDA and ISO regulations for medical device manufacturing.
- Communicate effectively with internal and external stakeholders, utilizing strong presentation skills.
- Remain calm and decisive under high-stress situations, making logical, resource-based decisions.
Schedule:
Monday-Friday, 6:00 AM - 4:00 PM
Job Experience
- 5+ years of leadership experience in a manufacturing setting.
- Familiarity with GMP for Medical Devices, FDA 21 CFR Part 820, and ISO 13485 standards preferred.
- Proven ability to manage production processes, lead teams, and achieve operational goals.
- Strong organizational, leadership, and problem-solving skills.
- Experience with MRP systems and key business indicators like quality, cost, and delivery metrics.
Job Education
Bachelor’s degree in Business, Engineering or a related field preferred.
Kentwood, MI
Susan Delauter
Susan.Delauter@SRGexpress.com
616-608-9681
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