What are the responsibilities and job description for the Senior Software Quality Engineer position at Werfen North America?
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
To be determined based on department needs, to include interactions such as:
The ideal candidate for this position will exhibit the following skills and capabilities:
Minimum Knowledge & Experience Required for the Position:
Education: Bachelor’s degree or equivalent in engineering or science.
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
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. Imple-ments 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.
- N/A
To be determined based on department needs, to include interactions such as:
- Works closely with other functions to generate compliant documents by interpreting and explai-ning 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 en-hanced compliance.
The ideal candidate for this position will exhibit the following skills and capabilities:
- Working knowledge of domestic and international quality/regulatory standards related to our pro-ducts
- Knowledge of quality management techniques (Lean, Six Sigma) and statistical techniques requi-red 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 re-quirements to data review, reports, design changes, risk management, etc. to ensure compliance and achieving business objectives. Demonstrated understanding of risk based approach to proces-ses and decisions.
Minimum Knowledge & Experience Required for the Position:
Education: Bachelor’s degree or equivalent in engineering or science.
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
- Approximately 10%
