Pave Talent is partnering with a world-class ISO 13485 certified medical device contract manufacturer. Our client, established in 1921, has grown to become an industry leader in innovative medical device components and assemblies, serving both global healthcare leaders and cutting-edge startups.
About Our Client
- Full-service medical device contract manufacturer
- ISO 13485 certified facility
- 100+ years of manufacturing excellence
- Company size: 51-200 employees
- Multiple US manufacturing locations
- Specializes in advanced molding technologies and medical device assembly
Position Overview Our client seeks a Process Lead for their Largo, FL facility to manage third-shift operations. This role combines hands-on technical expertise with leadership responsibilities, focusing on process optimization and team management.
Core Technologies
- Liquid Silicone Rubber (LSR) Molding
- Two-Material Molding
- Micro-Molding
- Silicone Extrusions
- High Consistency Silicone Rubber Molding
- Implantable Thermoplastic Molding
Schedule & Compensation
- Hours: Sunday (10:00 PM - 7:30 AM), Monday-Friday (11:00 PM - 7:30 AM)
- Base Pay: $33-36/hour
- Quarterly bonus program
- Comprehensive benefits package
- Company events and team activities
Key Responsibilities ?
- Lead third-shift operations and supervise production team
- Implement and optimize new manufacturing processes
- Focus on production launches and variation reduction initiatives
- Manage preventive maintenance programs
- Drive continuous improvement initiatives
- Partner with site management on strategic projects
- Ensure product quality and compliance with ISO 13485 standards
- Collaborate on Design for Manufacturability processes
- Support global supply chain initiatives
Required Qualifications
- Minimum 1 year of injection molding processing experience
- Proven expertise in plastic or silicone molding processes
- Strong mechanical aptitude with maintenance capabilities
- Experience with electrical, mechanical, pneumatic, and hydraulic systems
- Personal tool set required
- Demonstrated leadership and team management skills
- Excellence in problem-solving and critical thinking
- Commitment to quality and safety standards
Preferred Qualifications
- Technical education in Plastics Engineering, Engineering, or Polymer Science
- Experience with LSR processing
- Knowledge of medical device manufacturing
- Familiarity with automation and robotics (Nook/cobots)
- Clean room manufacturing experience
- Understanding of FDA requirements and ISO standards
Our client is an equal opportunity employer, committed to creating a diverse and inclusive workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
To be considered, candidates must:
- Submit a comprehensive resume
- Complete a culture index assessment (provided during the interview process)
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