Quality Engineer II — Onsite Medical Device Quality

BioCT Innovation Commons; North Haven (CT); On-site; USD 79,000 - 119,000; Full time

Benefits offered by this job

Health, dental and vision insurance

401(k) plan with employer match

Tuition assistance/reimbursement

Job summary

Medtronic is seeking a Quality Engineer II for its Surgical Sutures’ Manufacturing group in North Haven, CT. The role focuses on maintaining quality standards, collaborating with engineering and manufacturing, and ensuring regulatory compliance in medical device production.

You will work in a 100% onsite environment, five days a week, with cross-functional teamwork to enhance product reliability and process optimization.

Qualifications

• Bachelor’s degree in Engineering, Science or technical field with 4+ years of work experience in Engineering and/or Quality OR Advanced degree with 2+ years OR PhD with 0 years.

Responsibilities

• Develop, modify, apply and maintain quality standards and protocol for processing materials into finished or partially finished products.
• Collaborate with engineering and manufacturing functions to ensure quality standards are in place.
• Devise and implement methods and procedures for inspecting, testing and evaluating the precision of products and production equipment.
• Design or specify inspection and testing mechanisms and equipment; conduct quality assurance tests; perform statistical analysis to determine responsibilities for non-conforming products.
• Ensure corrective measures meet reliability standards and documentation is compliant with requirements.
• May specialize in design, incoming material, production control, product evaluation and reliability, inventory control or R&D as they apply to quality.

Skills

Quality engineering

Minitab

Six Sigma

CAPA

Process validation

Education

Bachelor’s degree in Engineering, Science or technical field

Advanced degree in Engineering, Science or technical field

PhD with 0 years relevant experience

Job description

Medtronic is seeking a Quality Engineer II for its Surgical Sutures’ Manufacturing group in North Haven, CT. The role focuses on maintaining quality standards, collaborating with engineering and manufacturing, and ensuring regulatory compliance in medical device production.

You will work in a 100% onsite environment, five days a week, with cross-functional teamwork to enhance product reliability and process optimization.