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Quality Assurance Technician, Medical Device Development
- Contract
- Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP)
- 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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