Job Summary:
Seeking a Quality Engineer with medical device experience to support and manage Quality Management System (QMS) compliance and documentation.

Job Requirements:

2-5 years of experience in the medical device industry Strong understanding of ISO 13485 Quality Management System (QMS) Solid knowledge of regulatory standards, including ISO 13485, MDR, and FDA requirements Experience managing Quality Management System documents and systems

Preferred Skills:

Proven ability to work cross-functionally with Engineering and Quality teams

Job Responsibilities:

Ensure compliance with ISO 13485 QMS and other regulatory standards Manage and maintain Quality Management System documentation Collaborate with cross-functional teams to uphold quality standards and compliance

Pay Details: $36.00 to $48.00 per hour

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

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The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
The California Fair Chance ActLos Angeles City Fair Chance OrdinanceLos Angeles County Fair Chance Ordinance for EmployersSan Francisco Fair Chance Ordinance