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Validation Engineer – Medical Device

Job in Hagerstown, Washington County, Maryland, 21749, USA
Listing for: EnIn Systems
Full Time position
Listed on 2026-02-12
Job specializations:
  • Engineering
    Quality Engineering, Systems Engineer, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

1 week ago Be among the first 25 applicants

Direct message the job poster from EnIn Systems

Actively Hiring Embedded S/W engineer ( Only on W2) ( All thevisa's are Recommended)

Key Responsibilities:

  • Develop and execute IQ/OQ/PQ protocols for equipment, utilities, and manufacturing processes in a medical device environment.
  • Plan and perform process validation, test method validation, and software validation (CSV) activities.
  • Author and review Validation Master Plans (VMP), Risk Assessments, URS, FRS, Traceability Matrices, and Validation Reports.
  • Collaborate with R&D, Quality Assurance, Regulatory Affairs, and Production teams to ensure validation deliverables align with product and process requirements.
  • Conduct design verification and validation testing (DV&V) for medical devices as part of design control.
  • Support regulatory audits and inspections by providing validation documentation and technical expertise.
  • Manage and document deviations, CAPAs, and change controls related to validation activities.
  • Maintain compliance with FDA QSR, ISO 13485, and GMP guidelines throughout the validation lifecycle.

Required Skills & Qualifications:

  • Bachelor’s degree in Biomedical, Mechanical, Electrical, or related Engineering discipline.
  • 3+ years of hands-on validation experience in the medical device industry.
  • Strong knowledge of GMP, FDA 21 CFR 820, ISO 13485, ISO 14971, and risk-based validation approaches.
  • Experience developing and executing equipment, process, cleaning, and computer system validation protocols.
  • Excellent documentation, analytical, and problem-solving skills.
  • Good communication and cross-functional team collaboration abilities.

Preferred Qualifications:

  • Familiarity with electromechanical and embedded medical device validation.
  • Experience with software validation under FDA and IEC 62304 guidelines.
  • Working knowledge of Track Wise, Master Control, or Veeva Vault for documentation management.
  • Certification in CQE, CQA, or RAC is a plus.
Seniority level
  • Seniority level

    Mid-Senior level
Employment type
  • Employment type

    Full-time
Job function
  • Job function

    Engineering and Information Technology
  • Industries Software Development and IT Services and IT Consulting

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