Quality Engineer

Amphenol Alden Products Company

  • Stoughton, MA
  • 21 days ago
  • $75,000–$85,000

Highlights

Job Summary: The medical device quality engineer supports the development, manufacture, and ongoing compliance of medical devices with a regulated quality management system. We recognize that our employees are at the cornerstone of our future, and we prioritize exceptional benefits, competitive compensation, work/life balance, and career development.

Numbers & Facts

LocationStoughton, MA
Salary$75,000–$85,000

Description

Join Amphenol Alden and Make a Difference in Patient Care Worldwide! 

 

At Amphenol Alden, we're dedicated to providing critical support to patients globally. Every device we manufacture directly impacts someone's loved one, a responsibility we hold with utmost seriousness. With roots as a family business over 80 years ago, we maintain a dynamic, entrepreneurial spirit, even now as part of a global corporation. 

 

We recognize that our employees are at the cornerstone of our future, and we prioritize exceptional benefits, competitive compensation, work/life balance, and career development. 

Due to our continuous expansion, we're seeking talented individuals to strengthen our team. We currently have an exciting opportunity for a Quality Engineer  at our new Stoughton MA facility.

Job Summary: The medical device quality engineer supports the development, manufacture, and ongoing compliance of medical devices with a regulated quality management system. This role is responsible for ensuring products and processes meet applicable regulatory requirements, internal quality standards, and customer expectations.

Primary Duties and Responsibilities:
• Work with engineering to develop inspection planning and documentation packages for customers.
• Work with customers regarding nonconformance, quality alerts and CAPA (problem solve).
• Execute First Article Inspections (FAI), CPK Studies, and GR&R

Skills/Qualifications Needed:
• Experience as a Quality Engineer in a manufacturing environment.
• Knowledge of ISO1348:16 and 21 CFR Part 820 Medical Device Requirements.
• Knowledge of PFMEA, Process Control Plans, Process Maps, other Engineering and Quality related processes.
• Knowledge of Validation (IQ, OQ, PQ)
• Computer skills: Word, Excel, PowerPoint, Minitab, etc.
• 4-Year College Degree; preferably in engineering or related.
• Ability to travel globally as needed to other AAP, supplier, and customer locations.
• Minimum 8-12 years' related experience in a manufacturing environment.
• Ability to travel as needed to other AAP, supplier, and customer locations.

Desired Skills:
• Lead auditor training to ISO13485:16 or ISO9001:15.
• Highly organized with excellent verbal and written skills, self-motivated.
• Understanding of REACH, ROHS, and Conflict Materials.

What We Offer:

•An opportunity to join a growing team dedicated to making a difference.

•Competitive salary, bonuses, and comprehensive benefits program, including medical, dental, vision, short and long-term disability, 401(K), PTO, HSA, FSA, employee discounts, life insurance, and employee activities.

Amphenol Alden Products is an Equal Opportunity Employer

 

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