Software Quality Assurance Engineer

  • location: San Diego, CA
  • type: Contract
  • salary: $50 - $53 per hour
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job description

Software Quality Assurance Engineer

job summary:
Looking for a Software Quality Assurance Engineer to help with ongoing business needs.

 
location: San Diego, California
job type: Contract
salary: $50 - 53 per hour
work hours: 8am to 5pm
education: Bachelors
 
responsibilities:
- Apply current inspectional techniques to project documentation during the system lifecycle and prior to FDA inspection and notified bodies to ensure a comprehensive documentation package is created and maintained.

- Interact and communicate (both oral and written) with junior project team/ organizational members, business leaders and senior executives.

- Effective judgment and decision making skills, typically made under stressful situations.

 
qualifications:
- Minimum 5 - 10 years of experience in software validation of R&D, Manufacturing and large scale computer systems (e.g. HP Quality Center, SAP, Trackwise, Enovia, Windchill, DOORS, etc.)

- Experience working in disciplined regulated industry in the application of automated technology particularly 21 CFR part 820, Part 11, ISO 13485, AAMI TIR 36, FDA Guidance, General Principles of Software Validation and GAMP 5.

- Competency in project management and the execution of multiple projects.

- Demonstrated capability in critical thinking and leadership with strong abilities in relationship management.

- Ability and willingness to travel 20% domestic and international.

- Fluent in English, Spanish is a plus but not required.

- Bachelor's degree (BSEE) in engineering and IT related fields; but any advanced degrees are preferable in Quality, Regulatory and Software Engineering.

 
skills: - Experience and Understanding of current inspectional practices of FDA, notified bodies and other regulatory agencies including previous interface with such bodies during regulatory assessments or inspections.

- Experience in leading and educating teams on the appropriate validation documentation created as objective evidence for software validations per company procedures, standards and regulations (e.g. 21 CFR part 820, Part 11, ISO 13485, AAMI TIR 36, FDA Guidance, General Principles of Software Validation and GAMP 5).

- Applied knowledge and understanding of (IQ) Installation Qualification, (OQ) Operational Qualification, (PQ) Performance Qualification, (UAT) User Acceptance Testing, (SAT) System Acceptance Testing.

- Ability to apply current inspectional techniques to project documentation during the system lifecycle and prior to FDA inspection and notified bodies to ensure a comprehensive documentation package is created and maintained.

- Demonstrated ability to interact and communicate (both oral and written) with junior project team/ organizational members, business leaders and senior executives.

- Effective judgment and decision making skills, typically made under stressful situations.


Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

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