Company: | MEDTRONIC |
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Job Role: | Biomedical Engineer II. |
Experience: | Freshers (0-2 years). |
Vacancy: | 10+ |
Qualification: | BE/B.Tech, ME/M.Tech, MBA or related degree. |
Salary: | $98,999 USD/year. |
Location: | North Haven - Connecticut - USA. |
Join us on Telegram | Click Here |
Apply Mode: | (Online) |
Deadline: | Not Mentioned |
- Conducts bench top, simulated tissue, and wet lab evaluations of prototypes.
- Analyzes data using statistical software and principles.
- Focus on the customer:
- Observes procedures in hospitals.
- Working closely with medical professionals, such as doctors, PAs, and nurses.
- Researches literature to stay up-to-date in the field.
- Team up with others cooperatively.
- Ensure that suitable testing is carried out to validate that the product meets customer and internal requirements. Collaborate with peers.
- Values and respects the opinions and ideas of team members.
- Ensures documentation is prepared in accordance with relevant internal SOPs and development process controls.
- Develops protocols and reports for studies during the method development, pre-verification, and verification phases of product development.
- Prepares posters and technical papers for presentations at technical and/or clinical conferences.
- Presents findings to peers, the leadership team, surgeons, customers and at society meetings.
- Effectively communicates with cross-functional teams.
- Effectively communicate with cross-functional teams.
- Bachelor's degree is required
- Minimum of two years of relevant experience, or an advanced degree with no experience
- Experience with medical devices or research is a plus.
- An understanding of anatomy related to MIS procedures.
- Biomechanics and mechanical testing principles and applications.
- Proficient in Microsoft Office; Word, PowerPoint, and Excel.
- Possess a can-do attitude and a "whatever it takes" attitude, as well as excellent organizational skills.
- Outstanding written and verbal communication skills/listening and presentation skills
- Detail-oriented with a strong commitment to quality and to the workplace, capable of multitasking.
- Knowledge of protocol writing and engineering reports for preclinical labs and engineering studies during the prevalidation and validation phase of a medical device.
- Knowledge of medical device regulatory pathways and experience gathering evidence for such.
- A pragmatic, solution-oriented thinker who possesses a "can do" and "whatever it takes" attitude along with excellent organizational skills.
- Analytical, communication [oral and written] and organizational skills are essential.
- Standard office setting, surgical lab, operating room, pilot lab, external research organizations, supplier visits, and limited travel as required.
- Located in the greater New Haven, CT area, USA
- Work 40 hours a week, Monday through Friday.
- Must be able to travel (up to 25% to 40%) of the time between New England facilities, primarily by car or train. Domestic travel will be required occasionally.
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