Analysis Skills, Biology, Cadence, Change Control, Change Management, Code of Federal Regulations, Communication Skills, Continuous Improvement, Cross-Functional, Data Quality, Documentation, FDA (Food and Drug Administration), FDA Requirements, GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), ISO (International Organization for Standardization), Lean Six Sigma, Learning Management System (LMS), Maintain Compliance, Manufacturing, Microsoft Product Family, Multitasking, Performance Analysis, Performance Management, Process Improvement, Process Validation, Quality Assurance, Regulatory Compliance, Risk Analysis, Six Sigma Certification, Standard Operating Procedures (SOP), Technical Delivery, Validation Documentation, Validation Plan
At Cadence, we improve product performance by building solution-oriented partnerships with our customers and delivering highly technical, measurable outcomes across medical, life sciences, automotive, 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 Cranberry Twp., Sturgeon Bay, WI, Suffield, CT 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)
- Maintain detailed validation documentation. (VMPs, reports, SOPs)
- 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.