Description: Our Medical Device Team is looking for an experienced Quality Engineer II and Quality Engineer IV to help work with our Engineering teams to ensure products are developed to exceed Customer expectations and requirement's.
Lead implementation of new/existing Quality assurance plans
Manage multiple projects and track deliverables
Must have strong documentation and proper writing skills
Ability to follow ISO 13485, MDR, and other regulations
Bachelor's Degree in Engineering
3+ years working in a highly regulated environment
Auditing experience
Top Skills Details:
ISO 13485
CAPA
QMS implementation
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
About Actalent
Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.