Develops system
and subsystem-level requirements for medical devices that include electromechanical hardware, software, disposables, and labeling.
Reviews systems engineering related processes and ensures they are current with industry standards and regulatory requirements.
Contributes to other R&D system engineering activities as needed including risk management, architecture review, V&V strategy, and post-market surveillance.
Keeps abreast of new developments in the industry and translates those developments into new and viable options for the organization and customers.
Investigates issues to determine root cause using established problem-solving tools.
Ensures that research and design methodologies meet established scientific and engineering standards.
Participates in design activities to ensure overall system performance is considered in product design decisions.
Presents technical information in a clear and precise manner.
Works independently with latitude for individual judgment.
Exercises judgment within defined procedures and practices to determine appropriate action.

B.S. degree in Engineering or related field
Minimum of 5 years of related experience or equivalent combination of education and experience
Experience with product development within a regulated industry
Development of FDA governed medical devices compliant to ISO 13485, ISO 14971 and IEC62304 preferred
A solid understanding of theories and practices utilized by other disciplines outside of primary area of expertise
Strong verbal and written communications skills
Ability to operate independently and exercise good judgement.

401(k) plan with company contributions
Paid vacation
Holiday and personal days
Employee assistance program
Health benefits including medical, prescription drug, dental and vision coverage

Principal Engineer – Systems, Requirements

Key skills