Quality Assurance Technician, Medical Device Development job in New Haven, USA

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First Name*

Last Name*

Email*

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Job type: Contract

Discipline: Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP)

Location: United States

This vacancy has now expired. Please see similar roles below...

Quality Assurance Technician, Medical Device Development - Contract - New Haven, CT

Proclinical is actively seeking a Quality Assurance Technician for Medical Device Development. This is a contract role located in New Haven, CT.

Primary Responsibilities:

This role focuses on ensuring the quality of medical devices throughout the development process. The ideal candidate will have a keen eye for detail, a strong understanding of quality assurance processes, and a passion for contributing to the development of life-changing medical devices.

Skills & Requirements:

Strong understanding of quality assurance processes.
Excellent attention to detail.
Ability to work collaboratively with a team.
Strong problem-solving skills.
Excellent written and verbal communication skills.

The Quality Assurance Technician will:

Oversee the quality assurance process throughout the development of medical devices.
Conduct regular inspections and audits to ensure compliance with regulatory standards.
Collaborate with the development team to address any quality-related issues.
Document and report any non-compliance issues.
Contribute to the continuous improvement of quality assurance processes.

If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at s.briggs@proclinical.com

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

INDCQA

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