Responsibilities:
- Develops and initiates standards and methods for inspection, testing and evaluation on sub-system and system integration.
- Devises sampling procedures and designs and develops control plans and instructions for recording, evaluating and reporting quality.
- Develops and implements methods and procedures for disposition of discrepant material and devises methods to assess cost and responsibility.
- Compiles and writes training material and conducts training sessions on quality control and assurance activities.
- Supports Manufacturing Engineers and Program Managers with customer interfaces as necessary on quality related issues.
- Assures data availability and integrity for all quality related data.
- Assist with developing, applying, revising and maintaining quality standards for processing materials into partially finished or finished products.
- Designs and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and/or components.
- Analyses reports and returned products and recommends corrective action.
- Provides liaison to various regulatory bodies.
- Other duties as assigned by management.
Required Skills:
- 5+ years of experience in Medical Device or EMS manufacturing environment.
- 10+ years of experience in general manufacturing environment.
- Minimum a Bachelor degree in science or engineering.
- Preferred Qualifications (nice to have skills): Initiative, superior problem solving skills, results oriented, good decision maker, excellent analytically, extremely well organized, assertive and a team player with situational sensibility.
- Excellent communication skills.
Job Type: Full-time
Pay: Up to $80,000.00 per year
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Schedule:
Experience:
- manufacturing: 10 years (Preferred)
Work Location: In person