Validation Engineering

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Full-Time Employee - 40 hr/week - 8 Hour Shift P2 Cranberry Township, PA, US

At Cadence , we improve product performance by building solution-oriented partnerships with our customers and delivering highly technical, measurable outcomes across medical device and other advanced industries.

We’re an engineering company at heart—with over 75 engineers across our organization—and have built a legacy of over three decades of manufacturing excellence by doing what others consider impossible.

We are seeking a highly motivated Validation Engineer onsite at one of our five sites: Sturgeon Bay, WI, Suffield, CT, Staunton, VA or Cranston, RI sites, to lead and support validation activities across multiple projects at our facility.

This role is critical in ensuring compliance with regulatory standards (FDA, ISO 13485, 21 CFR Part 820), working closely with engineering, QA, and manufacturing teams.

Conduct risk assessments and manage change controls

Ensure regulatory compliance (GMP, GLP, CSV, data integrity)

Collaborate cross-functionally to support validation strategy and training

Monitor system performance and lead requalification activities

Contribute to process improvements and continuous improvement initiatives

Bachelor’s in Engineering, Life Sciences, or related field

3+ years’ experience in validation or quality in a regulated industry

Proficiency in Microsoft Suite; experience with validation software

Preferred: Lean/Six Sigma certification; Split between office and production floor. Requires clear communication, computer use, and occasional physical movement around facility.