Our Client, a very exciting Medical Device startup, are searching for a Quality Engineer II to join their growing team.
Please note: This role is fully onsite with no hybrid or remote working options.
Responsibilities include but are not limited to the following:
Support the Quality Management System (QMS) to ensure compliance with regulatory standards and internal requirements.
Conduct and assist in internal audits and supplier evaluations.
Manage supplier relationships and ensure supplier compliance with quality standards.
Oversee product support activities, including batch release, test reporting, and first article inspections (FAI).
Collaborate with cross-functional teams to ensure product quality from early development stages through to commercial launch.
Implement and maintain effective processes for supplier management and evaluation.
WeSalute
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Veeva Systems
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