LINQM is looking for a Software Quality Engineer from the Medical Device or Pharma Industry.
Responsibilities for this position include:
- Work under the direction of a Software Quality Engineer to perform remediation activities and assist with gap analysis of legacy documentation to current standards.
- Create Master Validation Plans to complete remediation activities.
- Perform day to day software quality activities to ensure that product software and supporting test tools have been verified and validated (V&V) demonstrating that the software meets specification requirements and works as intended per user needs and systems requirements.
- Ability to use electronic system to manage our product Software Development Life Cycle (SDLC); including Defect Management, Risk Management and Software Configuration Management activities.
- Review and Approve Requirements Documents, Software V&V Test Protocols, Unit, Code Review and Test Summary Report(s).
- Ensure compliance with department and company procedures and instructions.
Skills:
- We are looking for an individual who has strong technical and communication skills, takes initiative, and demonstrates ability to work with cross functional teams as part of a project team.
- Willing to work in a fast paced dynamic environment to meet the needs of the business and deliver safe quality products to our patients
- Highly detailed, interpersonal skills, and ability to defend quality assurance is required.
- Excellent written and verbal communication skills.
Education:
- Must have a Bachelor’s degree in Sciences or Engineering or equivalent work experience of three (3) years.
- Requires a minimum of two (2) years in the Medical Device or Pharma industry.
- Experience in software development, software quality and/or software V&V is required.
- Must have labview experience