Production Sub-Lead: Medical Device Assembly & Training

Stryker Group; Irvine (CA); On-site; USD 33,000 - 44,000; Full time

Benefits offered by this job

Bonus eligible

Benefits

Job summary

Stryker Group in Irvine, CA is seeking a Production Sub-Lead to perform a series of assembly and test operations on medical devices, using tools, fixtures and test equipment. You will monitor production activities and assist the Lead in resolving issues.

You will also train and coach assemblers, delegate tasks with deadlines, enforce safety and quality policies, and maintain orderly work areas while following detailed instructions and regulatory requirements.

Qualifications

• High school diploma or equivalent.
• 2+ years experience in relevant role.

Responsibilities

• Monitor and help facilitate Production team activities and assist Lead in resolving Production problems.
• Instruct, train, and coach other Assemblers on procedures.
• Assist Lead in delegating tasks and setting deadlines and help enforce all safety and processing procedures.
• Understand and follow detailed assembly instructions, processes and procedures.
• Comply with policies, guidelines, and regulatory requirements per the Quality System.
• Report problems with quality, processes, equipment, and materials to Project Engineer and/or Lead.
• Provide hands-on job function training to coworkers as needed.
• Maintain a clean and organized work area to facilitate manufacturing functions.

Skills

Leadership experience

Coaching

Microscope assembly

Measuring techniques

Education

High school diploma or equivalent

Job description

Stryker Group in Irvine, CA is seeking a Production Sub-Lead to perform a series of assembly and test operations on medical devices, using tools, fixtures and test equipment. You will monitor production activities and assist the Lead in resolving issues.

You will also train and coach assemblers, delegate tasks with deadlines, enforce safety and quality policies, and maintain orderly work areas while following detailed instructions and regulatory requirements.