Non-Product Validation Engineer

Pacer Group

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profile Job Location:

Plano, TX - USA

profile Monthly Salary: Not Disclosed
Posted on: 6 hours ago
Vacancies: 1 Vacancy

Job Summary

Job Title: Non-Product Validation Engineer

Job location: Plano TX

Job Duration: 3 months contract to Hire

Job Description:

  • We are seeking a detail-oriented Non-Product Software (NPS) Validation Engineer to join our medical technology team.
  • This role is responsible for ensuring that all non-product software systems used in our quality management system processes comply with ISO 13485 standards and applicable regulatory requirements.
  • The ideal candidate will have strong technical skills combined with a thorough understanding of medical device quality systems validation methodologies and embedded systems experience.

Key Responsibilities:

  • Plan execute and document validation activities for non-product software systems in accordance with ISO 13485 requirements
  • Develop validation protocols including requirements specifications risk assessments test plans and validation reports
  • Conduct gap analyses of existing systems against regulatory requirements
  • Create and maintain validation documentation including traceability matrices
  • Collaborate with IT Quality and other cross-functional teams to ensure software systems meet business needs while maintaining compliance
  • Participate in internal and external audits related to software validation
  • Support change control processes for validated systems
  • Develop and implement validation strategies for new software implementations
  • Monitor and evaluate system performance to ensure continued validated state

Required Qualifications:

  • Bachelors degree in Engineering Computer Science or related technical field
  • Minimum 5 years of experience in software validation within a regulated medical device environment
  • Demonstrated knowledge of ISO 13485 requirements for non-product software validation
  • Proficiency in risk management techniques (FMEA FTA) as applied to software systems
  • Strong understanding of 21 CFR Part 11 compliance for electronic records/signatures
  • Excellent documentation and technical writing skills
  • Strong analytical and problem-solving abilities
  • Effective communication skills with the ability to explain technical concepts to non-technical stakeholders

Preferred Qualifications:

  • Masters degree in related field
  • Knowledge of additional regulatory frameworks (FDA QSR EU MDR MDSAP)
  • Background in computer system validation methodologies
  • Experience with validation of computerized systems in medical device environments
  • Familiarity with embedded software development lifecycles
Job Title: Non-Product Validation Engineer Job location: Plano TX Job Duration: 3 months contract to Hire Job Description: We are seeking a detail-oriented Non-Product Software (NPS) Validation Engineer to join our medical technology team. This role is responsible for ensuring that all non-product...
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Key Skills

  • Python
  • SOC
  • Debugging
  • C/C++
  • FDA Regulations
  • Minitab
  • Technical Writing
  • GAMP
  • OS Kernels
  • Perl
  • cGMP
  • Manufacturing