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...
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
View more
View less