Description:

　　The Sr Validation Engineer will be supporting the Quality team to support product launch to assure equipment and validation records are compliant from a quality perspective.

　　Requirements:

　　-8-12+ years of experience in validation engineering

　　-Minimum of 2+ years in Medical Device industry

　　-Equipment validation (IQ/OQ/PQ)

　　-Test Method Validation/Validation Master Plans

　　-Automated systems or equipment highly preferred

　　 Skills:

　　IQ/OQ/PQ, test method validation, master validation plans, Equipment validation, Validation protocols, quality processes, Medical device

　　Top Skills Details:

　　IQ/OQ/PQ, test method validation, master validation plans, Equipment validation

　　Additional Skills & Qualifications:

　　-documentation (validation protocols)

　　-Medical Device (ISO 13485)

　　-Quality Process/Engineering

　　Experience Level:

　　Expert Level

　　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.