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.