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Validation Engineer

Job in Grand Rapids, Kent County, Michigan, 49528, USA
Listing for: Performance Validation
Full Time position
Listed on 2025-12-06
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer, Biomedical Engineer, Process Engineer
Salary/Wage Range or Industry Benchmark: 75000 - 84000 USD Yearly USD 75000.00 84000.00 YEAR
Job Description & How to Apply Below

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Performance Validation provided pay range

This 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 types

Stock 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 Us

Here 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.

About

the 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
Requirements you will need Education
  • BS/BA degree and a minimum of two years in medical device validation
  • BS degrees in Biomedical Engineering, Chemical Engineering or Mechanical Engineering preferred
Experience
  • 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
What we have to offer
  • 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 Level

Associate

Employment Type

Full-time

Job function

Engineering and Consulting

Industries

Medical Equipment Manufacturing and Engineering Services

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