Join a team with a passion for innovation.

If you yearn to test the limits of your imagination and enjoy working in a casual, creative atmosphere, contact Nectar. Our team includes people with diverse backgrounds who contribute to every phase of product development. If you enjoy solving problems, tackling challenges, and working in a fast-paced, fun environment, we want to hear from you. Check out our current openings below.

Job Postings

IT Support Specialist

The IT Support Specialist is responsible for providing information solutions in hardware, software, network and installation support on desktop Personal Computers (PC) and other network computing devices.  Manages, maintains and updates servers, computers and internal network.  Ensures company security & backup policy, procedures and methods are up to date and properly implemented to protect company and client digital assets.  Overall the person must provide technical expertise to evaluate, install and maintain both hardware and software solutions to accurately meet the company‚Äôs needs.

Lead FW Engineer

The Lead FW Engineer will primarily execute and lead the Firmware aspects of projects.  The role is customer facing and requires the ability communicate technical details to potentially non-technical clients.  The role must also translate client needs to a technical team in order to plan, estimate, identify and manage tasks.  This role is expected to both develop FW and ensure delivery of technical goals of a team of resources, both internal and externally, on time and within budget.

Mechanical Engineer

The Mechanical Engineer will provide technical engineering leadership during the investigation, definition, design, development, and qualification phases of product development.

Quality Manager

The purpose of this position is to assume primary responsibility for the ISO 13485 registration and maintenance of the Nectar PD organization. The Medical Quality Engineer is responsible for ensuring the product development service and support activities of medical devices produced meet the requirements of 21 CFR Part 820, ISO 13485, the Medical Device Directive and other applicable regulations and standards. This position supports the operations team (design & engineering) through all phases of our medical products lifecycle. In addition, involvement with the internal audit process is required. This is a part time position.