Senior Software Quality Engineer
Senior Software Quality Engineer
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Job Description
Overview
Position Summary:
The Senior Software Quality Engineer position is responsible to ensure that activities throughout the product lifecycle are in compliance with procedures standards and regulations applicable to our products. In this capacity the Sr SWQE independently develops applies and implements methods tools and practices while working with project teams to achieve product quality goals and requirements in the areas of design development cybersecurity verification and validation maintenance and service. This is a technically focused role requiring advanced skills in analyzing information reviewing technical reports promoting process improvement requirements development risk management product development verification and validation and cybersecurity.
Responsibilities
Key Accountabilities
- Participates in the generation of quality documents throughout the product lifecycle.
- Advises and directs teams regarding compliance to procedures standards and regulations. Implements changes to procedures in alignment with evolving regulations.
- Ensures product quality meets requirements and documentation is complete prior to approval.
- Participates on core teams supporting new product development or design changes.
- Reviews and approves quality documents throughout the product lifecycle
- Supports audits and corrective actions to improve and maintain compliance of the QMS
- Identifies compliance gaps and takes appropriate corrective actions as needed
- Participates in and may lead quality system improvement projects as required.
- Performs other duties and responsibilities as assigned. Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Budget Managed (if applicable):
- N/A
Internal Networking/Key Relationships:
- Works closely with other functions to generate compliant documents by interpreting and explaining quality procedures applicable standards regulations and best practices.
- Able to effectively communicate quality requirements to a broad population of constituents.
- Ability to negotiate and influence others in establishing direction toward improved quality and enhanced compliance.
Skills & Capabilities:
- Working knowledge of domestic and international quality/regulatory standards related to our products
- Knowledge of quality management techniques (Lean Six Sigma) and statistical techniques required to measure and confirm significant changes.
- Working knowledge of products technology and manufacturing processes including impact on customers and patient requirements.
- Demonstrates judgement commensurate with experience regarding application of regulatory requirements to data review reports design changes risk management etc. to ensure compliance and achieving business objectives. Demonstrated understanding of risk based approach to processes and decisions.
Qualifications
Minimum Knowledge & Experience Required for the Position:
Experience: A minimum of 8 years of experience in medical devies pharmaceuticals diagnostic industry or clinical laboratory of 5 years of experience.
Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement.
International Mobility Required:
- No
Travel Requirements:
- Approximately 10
Required Experience:
Senior IC
Employment Type
Full-Time
