Sr. Clinical Engineer - EP Mapping Specialist
- Saint Paul, MN
- $75,300-150,700 per year
- Permanent
- Full-time
- Career development with an international company where you can grow the career you dream of.
- Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
- An excellent retirement savings plan with a high employer contribution
- Tuition reimbursement, the
- A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
- Provide feedback and insight on clinical workflows and clinical use of EP products.
- Support development of risk management documentation.
- Design, conduct/supervise, and support bench and preclinical studies for product concept feasibility and formal regulatory submission.
- Plan, coordinate, and conduct empirical and experimental analysis. Organize and analyze data from experiments or design builds and write reports on results.
- Conduct research and prepare research tasks.
- Document work suitable for technical papers and patents.
- Participate in project design reviews and project planning. Track performance against plan. Develop plan in conjunction with technical supervisor.
- Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
- Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
- Perform other related duties and responsibilities, on occasion, as assigned.
- Bachelors Degree (± 16 years) in Biomedical Engineering, Electrical Engineering, a related engineering field or an equivalent combination of education and work experience.
- Masters Degree (± 18 years) in relevant discipline/concentration, including Biomedical Engineering, preferred.
- Minimum 6 years relevant, progressively more responsible work experience in medical product development and/or a graduate degree with relevant project experience.
- Clinical EP experience as an EP tech, EP nurse, or in an industry EP field clinical support position with RCIS, RCES, CCDS, or CEPS certification; or, Design Validation and GLP study experience in the medical device industry.
- Demonstrated ability to apply an expert understanding of clinical application to issues in order to bring tasks to resolution within assigned projects. Demonstrated ability to effectively integrate information from varied disciplines including Clinical Medicine, Engineering, Marketing and Regulatory Affairs required. Medical device industry experience preferred. Training and experience in manufacturing processes and methods preferred.
- Experience working in a broader enterprise/cross-division business unit model preferred. Ability to work in a highly matrixed and geographically diverse business environment. Ability to work within a team and as an individual contributor in a fast-paced, changing environment. Ability to leverage and/or engage others to accomplish projects. Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. Multitasks, prioritizes and meets deadlines in timely manner. Strong organizational and follow-up skills, as well as attention to detail.
- Ability to travel approximately 5%, including internationally.