Principal Design Quality Engineer - Transfusion and Transplant jobs in United States
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Werfen North America · 9 hours ago

Principal Design Quality Engineer - Transfusion and Transplant

Werfen North America is looking for a Principal Design Quality Engineer to lead quality improvement initiatives and ensure product quality throughout the design and development process. The role involves authoring quality plans, overseeing compliance with regulatory requirements, and mentoring other quality engineers while fostering a culture of safety and quality.

Health CareManufacturing
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H1B Sponsor Likelynote

Responsibilities

Authoring and overseeing quality plans that meet compliance standards, including those related to product design, safety and reliability
Leading the process to ensure designs adhere to regulatory and quality requirements, including risk management activities
Overseeing design verification and validation activities, including testing, analysis and reviews
Leading and driving continuous improvement initiatives to enhance product quality, efficiency and customer satisfaction
Providing leadership and mentor-ship to other engineers, fostering a culture of quality and safety
Lead risk management initiatives for the entire product life-cycle in accordance with ISO 14971 and related regulatory requirements. Assure applicable quality decisions are derived from the appropriate risk management document in accordance to the quality system
Support on-going product compliance technical documentation and on-going market authorization through review and response to competent authority feedback in a timely manner
Support teams to establish product development requirements (e.g. Design Input documents, design verification and validation requirements, risk management requirements, usability requirements, CTQ Identification, etc.)
Serve as a Quality core team member on sustaining product life-cycle projects and new product development teams. Represent Quality for new and existing product improvement, manufacturing transfers, and quality plan initiatives
Performs other duties and responsibilities as assigned

Qualification

Quality managementRisk managementMedical device experienceTeam collaborationProblem solvingMicrosoft OfficeWritten communicationOral communication

Required

Minimum Bachelor's degree in Engineering (Bio Medical Preferred) or related scientific field
7 yrs minimum (Preferably Medical Device Industry)
Able to work in a team environment and collaborate
Demonstrates knowledge of products, services, procedures, policies, systems and company organization as it relates to job requirements
Display PC skills with Microsoft Office (Word, Excel) and other desktop functions at an intermediate level
Strong written and oral communication skills (timely, clear, concise, accurate, conclusive, influential, targeted to audience
Excellent teamwork skills including influencing and building rapport with internal departments and stakeholders
Excellent problem solving skills, including demonstrated critical thinking skills and application of structured problem solving methods and tools
Able to lead and make independent decisions in collaboration with cross functional teams

Company

Werfen North America

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Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain.

H1B Sponsorship

Werfen North America has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (10)
2024 (12)
2023 (10)
2022 (2)
2021 (11)
2020 (8)

Funding

Current Stage
Late Stage

Leadership Team

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Giovanni Russi
Chief Operating Officer
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Dominique J.
Human Resources Business Partner
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Company data provided by crunchbase