Manager, Design Quality Engineering

• Leads quality team on product development projects, executing functional deliverables and ensuring technical excellence in the achievement of organizational goals. Key Quality voice of influence on projects.
• Owns and drives deliverables related to Design Controls, Risk Management, Product Performance, Quality, and Compliance.
• Develops and implements quality strategies; seeks innovative approaches to attain quality goals.
• Drives functional excellence in Quality Engineering by developing, coaching, and mentoring team members.
• Maintains and enhances cross-functional team relationships.
• Provides significant guidance regarding technical strategies and approaches; works cross-functionally in identifying and resolving technical issues.
• Drives continuous improvement in enabling processes, especially Design Controls and Risk Management.
• Develops department budget and monitors spending. Works with key partners to understand priorities and plans resource allocation accordingly.
• Fosters a diverse and inclusive workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives.
• Monitors and ensures compliance with company policies and procedures.
• Audit Mastery: Plan and execute detailed audits across various project phases to ensure compliance with Verathon standards and contract requirements. Manage follow-up activities for internal audits, ensuring corrective actions are effectively implemented.
• Must have the ability to travel to the US regularly without restrictions.

• Bachelor’s degree in a related scientific or technical discipline is required; Masters preferred
• Typically requires a minimum of 5 years' experience in quality engineering or new product development within a regulated industry (e.g., medical devices, pharmaceuticals, biotechnology, or healthcare products).
• A minimum of 2 years of people management is required.
• Demonstrated proficiency and knowledge of current medical device Good Manufacturing Practices 21CFR820, FDA 510(k), and EU Medical Device Regulation.
• Experience with IEC 60601, device cybersecurity, and/or sterile single-use devices desirable
• Must possess excellent leadership skills with ability to work effectively in cross-functional teams in a dynamic, fast-paced environment.
• Demonstrated ability to build, engage and develop a team to sustain a productive and positive working environment.

• For applicants without an Engineer in Training or a Professional Engineer license, an alternative title will be used until a license is obtained. Verathon is proud to provide job-related professional growth and development of employees, including reimbursements for expenses incurred in joining the EGBC.

• Be part of an innovative team that is dedicated to improving patient outcomes.
• Engage in meaningful work that makes a difference in the healthcare industry.
• Competitive salary and comprehensive benefits package.

• Salary range - $131,950 - $175,200 (Compensation will vary based on skills, experience and location; it is not typical to be hired at or above the top of the salary range).
• Full-time employees who are not on a commission plan are eligible for Verathon’s annual bonus plan based on company and individual performance.
• Verathon provides a competitive benefits package including a generous HCSA, paid holidays, paid time off and a retirement matching plan.

Verathon