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Quality Engineer

  • ... Posted on: Jan 14, 2025
  • ... TekWissen LLC
  • ... Walpole, Massachusetts
  • ... Salary: Not Available
  • ... Full-time

Quality Engineer   

Job Title :

Quality Engineer

Job Type :

Full-time

Job Location :

Walpole Massachusetts United States

Remote :

No

Jobcon Logo Job Description :

Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide 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 follow-up care, empowering healthcare providers worldwide.
Job Title: Quality Engineer 2
Location: Walpole, MA, 02032
Duration: 7 Months
Job Type: Contract
Work Type: Onsite
Shift: 8.00 am to 5.00 pm EST
Job Description:
Specific Requirements
  • The Design Quality Engineer will participate in the governance, and execution of the Quality Management sub-system element of Design Chnage.
  • 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
  • 2-5 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.

Jobcon Logo Position Details

Posted:

Jan 14, 2025

Employment:

Full-time

Salary:

Not Available

Snaprecruit ID:

SD-CIE-400f4c8f63bdf6b89fa4d6447eb7941353a7c9a3ae99d7676d19d07c361898d2

City:

Walpole

Job Origin:

CIEPAL_ORGANIC_FEED

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Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide 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 follow-up care, empowering healthcare providers worldwide.
Job Title: Quality Engineer 2
Location: Walpole, MA, 02032
Duration: 7 Months
Job Type: Contract
Work Type: Onsite
Shift: 8.00 am to 5.00 pm EST
Job Description:
Specific Requirements
  • The Design Quality Engineer will participate in the governance, and execution of the Quality Management sub-system element of Design Chnage.
  • 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
  • 2-5 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.

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