Validation quality Engineer

Overview

$$50
Accepts corp to corp applications
Contract - Independent
Contract - W2
Contract - 6 Month(s)

Skills

Product software Quality
Design Controls
NPSW Validation
Risk Assessment & Mitigation
IEC 62034
ISO 14971

Job Details

Position: Validation quality Engineer

Location : San Diego CA

  1. Product software as a medical device verification and validation activities for new products (Quality Engineer supporting the R&D team).
  2. Medical device R&D product software .
  3. resource shall have a background in the medical/pharma domain.
  4. resource shall have product software validation experience and a minimum of 2 to 3 years of experience in Quality.

resource shall have experience as a Software Quality Engineer or Validation Engineer and Quality Engineer.

Job Summary:

  • Provides technical and quality system guidance related to establishing product software as a medical device requirements.
  • Provide quality oversight for product software as a medical device verification and validation activities for new products in accordance with design planning procedures. This includes, but is not limited to, reviewing and approving software test case protocols and reports, review of software development plans, and review of other system and software documentation.
  • Leads meetings to prioritize, review and/or approve of action plans for addressing issues captured in problem resolution systems during development.
  • Leads risk evaluation and associated management activities related to product software development including Risk assessments (e.g. FMEA), product risk analysis, and mitigation of software issues.
  • Participates in technical and management reviews to ensure design plans, product design and deliverables related to product software are met. Represent the quality engineering function for the review and approval of designated design controls.
  • May provide quality oversight for non-product software validation by assessing the need for validation and preparing and/or supporting protocols, reports and other documentation as required.
  • May be involved with supporting product cybersecurity assessments in conjunction with a cross-functional team
  • Complies with US FDA regulations, other country regulatory requirements, company policies, and procedures.
  • Maintains a strong, collaborative partnership with cross functional team members especially with software supplier.
  • Works as an individual contributor and may provide guidance of other QE team members.



Key word to search

Product software Quality, Design Controls, NPSW Validation, Risk Assessment & Mitigation, IEC 62034, ISO 14971
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.