Validation Engineer
Listed on 2025-12-06
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Engineering
Quality Engineering, Manufacturing Engineer, Biomedical Engineer, Process Engineer
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Performance Validation provided pay rangeThis range is provided by Performance Validation. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range$75,000.00/yr - $84,000.00/yr
Additional compensation typesStock options
Direct message the job poster from Performance Validation
Qualified candidates must be legally authorized to be employed in the United States. Performance Validation, Inc. does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position. About UsHere at Performance Validation, Inc (PV) we have been providing Commissioning, Qualification, and Validation services to the life science industries for over 36 years. We are a 100% employee owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, and North Carolina, and we support clients throughout the US and overseas. As an employer, PV is committed to providing growth opportunities to our employees through professional development, implementation of new services, and cultivation of new geographical areas.
Aboutthe job
Performance Validation is seeking a full-time Level 2 Validation Engineer/Specialist to join our team in Grand Rapids, Michigan. Level II Validation Engineer/Specialist reports directly to the Site Manager and will be assigned to one or more project teams headed by a Project Leader.
Responsibilities- Develop a sound understanding of how to properly implement technical, quality, and scientific principals necessary to meet industry and customer requirements
- Work in a team environment to meet defined objectives based on established timelines
- Develop verification/qualification deliverables including but not limited to Requirements Documents, Functional and Design Specifications, Test Protocols (IQ/OQ/PQ), and Summary Reports
- Execute test protocols, including identification and resolution of non-conformances/deviations
- Track and manage change control activities for multiple concurrent projects
- BS/BA degree and a minimum of two years in medical device validation
- BS degrees in Biomedical Engineering, Chemical Engineering or Mechanical Engineering preferred
- Self-starter who exhibits a professional demeanor, enthusiasm, and ability to work independently with minimal supervision
- Strong interpersonal skills. Must interact confidently with clients, other contractors, and employees
- Possess excellent oral and written communication skills and high attention to detail
- Experience with office word-processing and spreadsheet programs such as Microsoft Word and Excel
- Competitive base salary with opportunity for additional compensation based on hours worked
- Biannual profit share
- Employee stock ownership program
- 401(k) company match
- Flexible Time Off
- Internal and external training opportunities
- Medical, vision, and dental coverage
- Disability and life insurance
- Cellphone stipend
- Growth opportunities
- Company-sponsored team building outings
- A collaborative work environment
- Work/life harmony
Up to 20% availability to travel.
Seniority LevelAssociate
Employment TypeFull-time
Job functionEngineering and Consulting
IndustriesMedical Equipment Manufacturing and Engineering Services
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