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We are looking for a Senior Opto-Mechanical Engineer! NVIDIA's GPUs and SOCs are the world leaders in performance and efficiency, and we are continually innovating in creative and unique ways to improve our ability to deliver extraordinary solutions in a wide range of sectors. We are seeking mechanical engineers who are passionate about what they do and are committed to making a difference in the world through their inventions. This position will collaborate with mechanical, opto-mechanical, and process engineers in the design and development of components that will drive our products into a new technology era. Your responsibilities will include designing mechanical components and assembly platforms, selecting technology, and benchmarking solutions, all while keeping schedule and budget targets.

What you'll be doing:

Development of innovative microelectronics packaging of our Networking Business Units future products.

Mechanical design and design validation of micron-scale optical elements (lenses, connectors, etc.).

Mechanical design and solution for micron-scale assembly stations.

Work with world-leading vendors to develop highly ambitious packaging solutions.

Partner with engineering to solve problems during New Product Introduction enabling an efficient transition to Mass Production.

Join and lead task forces to investigate and support production excursions, failure analysis, and reliability issues.

We are looking for an innovative R&D Mechanical Design Engineer to join Our Mechanical Department!
Job description:
Managing the mechanical design of projects under development, from concept to completion.
Responsible for mechanics risk management and mitigation processes.
Executing the mechanical design of plastic parts and assisting throughout the mold production.
In charge of performing and documenting tests.
Performing design improvements and supporting production lines.

Mechanical Engineer within the Urology Division will be responsible for providing support for released products within the Laser Franchise, which consists of Holmium and CO2 laser capital systems, laser fibers and associated accessories.

Mechanical Engineer works in close collaboration with the different technical disciplines (Elec, Mech, SW, Physics), as well as the other cross-functional groups (Quality, Regulatory, Manufacturing, Service) to support sustaining activities as part of Product Life Cycle.

Mechanical Engineer supports growth of products to new markets and leads design changes originating in product improvements, regulatory or supply chain needs.

Main Duties:
Conduct root cause analysis of design related field complaints.
Lead product improvement design activities.
Provide technical assistance for sales and marketing activities.
Support the integration of acquired assets within the laser franchise into the company`s Scientific quality system.
Work in collaboration with Regulatory team to provide and maintain the regulatory design inputs and systems compliance. Own the transfer from regulation/standards to engineering derivatives (impact assessment and deployment).
Support RA team with new markets registrations and regulatory submissions.
Definition, writing and management of Design Inputs and flow down for the sustaining products.

The System Engineer Architect will play a key role in designing, developing, and optimizing advanced laser optical systems for Urology, as well as supporting ongoing activities as part of Product Life Cycle, while working in close collaboration with the lead Sys Eng., the different technical disciplines (Elec, Mech, SW, Algo), and other groups (RA, QA, Mfg).

Main Duties:
Support technical characterization and system design of cutting-edge laser systems.
Lead the architectural design of laser systems, including Tx-Rx design and SNR optimization, to meet performance specifications and customer requirements.
Conduct system-level analysis, simulations, and modeling to evaluate and validate system performance under various operating conditions.
Lead problem solving and escalations of system-level issues, proposing, and implementing effective solutions.
Understanding the range of user, product, business and marketing requirements, and work in collaboration with Sys Eng. to convert them to practical system level requirements.
Lead integration and lab experiments in collaboration with cross functional teams to validate and optimize system functionalities.
Analyze system performance data to derive meaningful insights and recommendations. Implement data-driven improvements.
Lead design reviews, project meetings, and technical discussions to communicate progress, challenges, and recommendations effectively.
Stay current with emerging technologies and industry trends in laser systems and signal processing and provide recommendations for technology adoption and innovation.
Mentor and provide technical guidance to junior engineers, fostering their professional growth and development.
Drive excellence, innovation, and efficiency in system design processes, ensuring reliability and performance meet the highest standards.

Highly skilled and motivated Quality Design Engineer to join our dynamic team in the medical device industry.

The ideal candidate will have a strong background in design control, quality assurance, and regulatory compliance, with the ability to work collaboratively with R&D, Engineering, Regulatory and other teams.
Adaptable and possess a deep understanding of the regulatory landscape governing medical devices, specifically experience in all phases of product life cycle (design, development, risk management, design verification, production) in adherence with ISO13485:2016, 21 CFR 820 and ISO14971.
Main Duties:
- Lead and implement design control and production processes to ensure compliance with industry standards and regulations.
- Lead proactive design assurance activities facilitating the development and release of high-quality products.
- Collaborate with cross-functional teams to integrate quality into the design and development and manufacturing process.
- Stay abreast of evolving regulatory requirements for medical devices and ensure the company's adherence to relevant standards.
- Work closely with R&D teams to understand design requirements and provide quality engineering input throughout the product development lifecycle.
- Conduct design reviews to identify and address potential quality issues early in the process.
- Responsible for reviewing, providing input and approving product development DHF documentation (design planning, inputs and outputs, design review, V&V protocol -reports, risk analysis, and design change, product transfer to operations, etc).
- Responsible for approval of product design changes and process changes (ECO).
- Participate in Design Reviews for product teams as the quality expert, reviewer, and approver.
- Implement risk management processes and methodologies in the design and development phases per ISO 14971.
- Participate in risk assessments and develop strategies to mitigate potential risks.
- Establish and maintain quality assurance procedures to ensure product quality and regulatory compliance.
- Conduct audits and assessments to identify areas for improvement and implement corrective actions.
- Conduct Failure investigations for Complaints and CAPA.
- Responsible for approval of equipment qualification and process validation documents (pFMEA, IQ, OQ, PQ, etc).
- Perform supplier audits and provided support in preparation and performance of external audits to ensure quality and regulatory requirements are met.
- Support continuous improvement activities to reduce product failure rates.