Senior Software Quality Engineer Position Available In Middlesex, Massachusetts

Senior Software Quality Engineer Werfen United States, Massachusetts, Bedford 180 Hartwell Road (Show on map) Jun 10, 2025
Job Information
Number

ICIMS-2025-8722

Job function
QA&RA
Job type
Full-time
Location
Bedford – 180 Hartwell Road Bedford, Massachusetts 01730 United States
Country
United States About the Position
Introduction Werfen Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.

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. 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. Budget Managed (if applicable):

N/A Internal Networking/Key Relationships:

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.

Skills & Capabilities:

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.
Qualifications 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 Travel Requirements:

Approximately 10% If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact NAtalentacquisition@werfen.com for assistance. We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team. www.werfen.com Apply Now