Quality Design Engineer

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

Are you looking to further your career and grow?

Do you have experience in a Quality Engineering within an FDA regulated industry preferably medical device and diagnostics?

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

Acara Solutions seeks highly qualified candidates to work Onsite for our client in Walpole, MA Interested?

Here's what you'll do:

• The Design Quality Engineer will participate in the governance, and execution of the Quality Management sub-system element of Design Change. Specifically, the person will be 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 as to support QT and other business initiatives including, but not limited to audits (internal / external), supplier quality, CAPA, and training.
• Participate as a core team member on various design changes
• Provide assistance to the engineering partners in the development of 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 & 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: $43.00 /Hour

Hours: 40 hours/week (1 shift)

Length: Contract (7 months)

Does that sound 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 or similar role within an FDA regulated industry preferably 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 required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.