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Senior Validation Engineer

Job in Lake Geneva, Walworth County, Wisconsin, 53147, USA
Listing for: Medix™
Full Time position
Listed on 2026-10-05
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
  • Engineering
    Quality Engineering, Regulatory Compliance Specialist, Process Engineer
Salary/Wage Range or Industry Benchmark: 85000 - 120000 USD Yearly USD 85000.00 120000.00 YEAR
Job Description & How to Apply Below
Position: Senior Validation Engineer - 171296
Key Responsibilities
  • Lead validation activities for manufacturing processes, equipment, and supporting systems.
  • Develop and execute validation documentation, including Validation Plans, URS, risk assessments, IQ/OQ/PQ protocols and reports.
  • Coordinate shop-floor execution of validation protocols, including resources, sampling, instrumentation, and testing.
  • Establish and evaluate critical process parameters, control limits, and process capability using DOE, MSA, SPC, and capability analysis.
  • Analyze manufacturing and validation data to identify trends and opportunities for improvement.
  • Lead root cause investigations, CAPA activities, and process improvement initiatives.
  • Support equipment qualifications, process changes, equipment transfers, and engineering changes while maintaining the validated state.
  • Partner with Manufacturing, Quality, Engineering, and other cross-functional teams on validation and process improvement activities.
  • Support improvements to quality systems, procedures, work instructions, and validation workflows.
  • Ensure appropriate data integrity and documentation practices within computerized systems.
  • Provide technical guidance and mentorship to engineers and technicians on validation practices, documentation, and statistical methods.
Qualifications
  • Bachelor's degree in Engineering, such as Mechanical, Manufacturing, Industrial, Biomedical, or a related field.
  • 6+ years of validation experience within a regulated manufacturing environment such as medical device, pharmaceutical, or combination products.
  • Strong experience with IQ/OQ/PQ and validation lifecycle activities.
  • Knowledge of cGMP, ISO 13485, 21 CFR 820, and Part 11; familiarity with GAMP 5 and risk-based validation is preferred.
  • Experience developing sampling strategies, acceptance criteria, and validation test methods.
  • Strong understanding of DOE, MSA/Gage R&R, SPC, and process capability analysis.
  • Experience using Minitab or similar statistical software.
  • Strong technical writing, documentation, and data integrity skills.
  • Experience with process/equipment qualifications, automated manufacturing, or cleanroom environments is preferred.
  • Strong communication skills with the ability to work effectively across cross-functional teams.
Work Environment:

This is an on-site position supporting manufacturing and validation activities directly on the production floor.

Position Requirements
10+ Years work experience
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