Ximedica

Opportunities


Systems Engineer

Ximedica is an ISO 13485:2012 certified and FDA registered full-service product development firm with offices in Providence, St. Paul, San Francisco, Los Gatos, and Hong Kong. We have an exclusive focus on medical products and over 25 years of experience developing medical devices, combination products and consumer healthcare products. We have a high-energy collaborative culture that fosters the creative spirit while exceeding client expectations. We offer tremendous opportunity for professional development and leadership, rewarding projects, competitive salaries, an excellent benefits package, and summer hours.

The Systems Engineer supports our domestic and international product development business.

Nature of Role: Reporting to the Head of Systems Engineering, the Systems Engineer is responsible for various systems engineering functions within multiple projects, including but not limited to interfacing with various disciplines such as user research and industrial design, translating user needs into requirements, requirements analysis and creation appropriate for engineering development, and leading and organizing systems architectures between the various engineering disciplines (including but not limited to Mechanical Engineering, Electrical Engineering, and Software Engineering architectures).

The System Engineer’s main objectives are to ensure proper translation of user, caregiver and a variety of additional stakeholders’ needs into clearly defined, verifiable design inputs. The engineer collaborates with project teams to define system solutions, architectures (design outputs) and interface output requirements between various subsystems to adequately meet the design inputs.

The engineer will collaborate with user research specialists to gather and prioritize stakeholder needs, work with clients to gather and prioritize both business needs and pre-defined design constraints. Early activities include determining the essential requirements necessary to drive initial concept development, leading systems architecture concept development sessions, and creating ratings criteria for concept ranking and acceptance of early architectural concepts. Parallel activities will include translating the early research findings and regulatory requirements into functional requirements with documented rationales, intended to be measurable and verifiable or validated at later stages. Late stage activities include advising on formal verification plans in collaboration with Design Assurance Engineers and assisting with test method dentification and development. The role will also require incorporation of directly related standards and regulatory requirements.

Responsibilities:

  • Lead systems engineering efforts and drive related deliverables on multiple project
  • Develop design input requirements, exercise analysis tools such as parsing, and ensure rationales are provided for requirements
  • Collaborate with user research specialists to gather and prioritize stakeholder needs
  • Work with clients to gather and prioritize business needs and pre-defined design constraints
  • Define essential requirements necessary to drive very early concept development
  • Lead systems architecture concept development sessions; create rating criteria for concept ranking and acceptance of early architectural concepts
  • Translate early research findings and regulatory requirements into functional requirements.
  • Capture the evolution and ultimate systems design output, rationales, and lower level requirements associated with final design
  • Contribute to formal verification planning in collaboration with assigned Design Assurance Engineers, and assist with test method identification and development
  • Keep abreast of related laws and regulations, and incorporate compliance within systems engineering deliverables
  • Participate in continuous improvement efforts related to systems engineering processes
  • Assist the Head of Systems Engineering with staff training on a periodic basis and teams on an as needed basis

Requirements:
An individual holding a bachelor’s degree in a related field, coupled with 2+ years of experience within the product development industry. Familiarity with related standards and medical device development is a plus. Our fast-paced environment demands the ability to manage multiple projects within the discipline and deadlines. High-energy, self-starters with the following qualities:

  • Successful communication skills, business acumen and assertive decision-making ability
  • Flexibility to multi-task and perform a wide range of activities
  • Excellent computer skills, including MS Office proficiency

Please note: JOB CODE #843PVDSFLG when applying.

 

Send resume to: HR@ximedica.com.

Apply Now

 

EQUAL OPPORTUNITY EMPLOYERXimedica provides equal employment opportunities to all qualified applicants and employees regardless of race, color, religion, gender, age, national origin, sexual orientation, veteran status, disability that can be reasonably accommodated, or any other basis prohibited by federal, state, or local law. 

Wherever you are in your process, Ximedica can help

Contact Us

At Ximedica, our people define who we are.

More About Our People

Marina Aldarondo

Marina Aldarondo

Human Centered Industrial Design & Marketing Strategist

John Torrey

John Torrey

Senior Quality Engineer

Marco Flavio Marinucci

Marco Flavio Marinucci

Director of Digital Products

Breck Petrillo

Breck Petrillo

Director of Engineering

Ben Vespone

Ben Vespone

Biomedical Engineer

Ken Focht

Ken Focht

Principal Mechanical Engineer