Product Development Engineer (w/m/d) 100 % - Moving Spine AG
at Universittsklinik Balgrist
Zürich, ZH, Switzerland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 17 Feb, 2025 | Not Specified | 18 Nov, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Our goal is to bring a new treatment category (Spine Sports Medicine) to the patient and to delay spinal fusion surgeries within the continuum of care for spinal disorders by introducing motion preserving stabilization techniques. Our instruments and implants will allow for novel, less invasive spinal treatments and faster patient recovery. We are a spin-off of the highly innovative Balgrist Campus, the Balgrist University Hospital and ETH Zürich. Moving Spine AG is a well-financed, disruptive start-up with a broad range of experienced external partners.
For our offices in Zürich Stadelhofen SBB and Balgrist Campus, we are looking for a motivated, innovative and creative
NEXT STEPS
For further information, please contact careers@movingspine.ch.
We’re looking forward to receiving your complete online application.
Moving Spine AG, Eisengasse 16, CH-8008 Zürich, Switzerland, www.movingspine.ch
How To Apply:
Incase you would like to apply to this job directly from the source, please click here
Responsibilities:
- Product Development: design and develop novel and disruptive spine instruments and implants according to ISO 13485, FDA and CE/MDR regulations and highest industry standards
- Customer Focus: Give input to design goals and specifications based on requirements and validated user needs in collaboration with product manager / project leader
- Technical Project Leader: Participate in technical efforts amongst internal and external partners (CROs, CMOs, design service providers, process development experts, prototype shops etc.
- Regulatory: Contribute to the entire Technical Documentation. Contribute technical design and project phase reviews. Support the risk documentation incl. FMEA, hazard analysis, risk management etc.
- Cross-Functional Contributions: Contribute to quality engineering, regulatory, supplier engineering, project management, manufacturing engineering, clinical, and product management
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Mechanical or Industrial Engineering
Engineering Design / R&D
Mechanical Engineering
Graduate
Proficient
1
Zürich, ZH, Switzerland