Quality Engineer 2
Quality Engineer 2
Posted on :
30-11-2024
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1 Vacancy
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Job Description
Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients worldwide. The below client is with one of our client which is a leading global medical technology company. It offers a wide range of diagnostic imaging and laboratory diagnostics as well as advanced therapies and digital health services. Its solutions span from prevention and early detection to diagnosis treatment and followup care empowering healthcare providers worldwide.
Job Title: Quality Engineer 2
Location: Walpole MA 02032
Duration: 9 Months
Job Type: Contract
Work Type: Onsite
Shift Timings: 8:00 am 5:00 pm EST
Job Description:
Specific Requirements:
- The Design Quality Engineer will participate in the governance and execution of the Quality Management subsystem element of Design Change.
- Specifically the person will be required 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 required to support QT and other business initiatives including but not limited to audits (internal / external) supplier quality CAPA and training.
Major Job Responsibilities
- 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
Required Knowledge/Skills Education and Experience
- 25 years of experience in a Quality Engineering or similar role within an FDA regulated industry preferably medical device and diagnostics that includes experience with CAPA and auditing processes.
TekWissen Group is an equal opportunity employer supporting workforce diversity.
Employment Type
Full Time
Key Skills
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