Design Quality Engineer

Are you a Design Quality Engineer looking to join one of the top companies in the Manufacturing industry?

Are you looking to further your career and grow?

Do you have experience in a Quality Engineering role within an FDA-regulated industry, including medical device and diagnostics?

If you answered yes to those three questions, then apply today!

Acara Solutions seeks highly qualified candidates to work on-site with our client in Walpole, MA. Interested?

Here's what you'd do:

• The Design Quality Engineer will participate in governing and executing the Quality Management subsystem element of Design Change.
• Specifically, the person will need to interact and collaborate with cross-functional teams to promote and drive Quality Systems compliance regarding product design and development activities.
• Additionally, this role will lead specific quality improvement projects to support QT and other business initiatives, including audits (internal/external), supplier quality, CAPA, and training.
• Participate as a core team member on various design changes.
• Assist the engineering partners in developing design verification and validation testing requirements, including protocol development, test methods, acceptance criteria, and statistical plans/techniques.
• Support the development, monitoring, and reporting of Quality Systems' key performance indicators (KPIs), which will include assisting in the development of Quality Goals and objectives across POC.
• Support internal and external audit needs while serving as the subject matter expert for Design Quality Assurance.

Here's what you'll get:

Pay: $43/hr.

Hours: 40 hours/week (1^st Shift).

Length: Temp (10 Months).

Sounds like a good fit?

APPLY TODAY

About Acara Solutions

Acara is a premier recruiting and workforce solutions provider-we help companies compete for talent. With a legacy of experience in various industries worldwide, we partner with clients, listen to their needs, and customize visionary talent solutions that drive desired business outcomes. We leverage decades of experience to deliver contingent staffing, direct placement, executive search, and workforce services worldwide.

• High School Diploma or GED.
• Minimum of 2 years experience in a Quality Engineering role within an FDA-regulated industry, including medical device and diagnostics.
• Minimum of 2 years experience with CAPA and auditing processes.

Additional Information:

• Upon offer of employment, the individual will be subject to a background check and a drug screen.
• In compliance with federal law, all persons hired will be needed to verify identity and eligibility to work in the United States and to complete the necessary employment eligibility verification form upon hire.