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Validation Engineer II

Job in Staunton, Augusta County, Virginia, 24402, USA
Listing for: Cadence Inc.
Full Time position
Listed on 2026-07-07
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 75000 - 95000 USD Yearly USD 75000.00 95000.00 YEAR
Job Description & How to Apply Below

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

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

30+ days ago Requisition

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.

Position Overview

We are seeking a highly motivated Validation Engineer onsite at one of our five sites:
Cranberry Twp., 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.

Key Responsibilities
  • Develop and execute validation protocols (IQ, OQ, PQ, TMV)
  • 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
  • Qualify suppliers and vendors
  • Contribute to process improvements and continuous improvement initiatives
Qualifications
  • Bachelor’s in Engineering, Life Sciences, or related field
  • 3+ years’ experience in validation or quality in a regulated industry
  • Knowledge of FDA, ISO 13485, 21 CFR Part 820 standards
  • Proficiency in Microsoft Suite; experience with validation software
  • Strong communication, documentation, and analytical skills
  • Preferred:
    Lean/Six Sigma certification; experience with LMS systems
Work Environment

Split between office and production floor. Requires clear communication, computer use, and occasional physical movement around facility.

We are not offering sponsorship at this time for this position.

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