CURRENT OPENINGS
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We are constantly searching for excellence. Below are the open opportunities that are in need of qualified candidates. Please read through the detail descriptions thoroghly and only apply if you are serious about wanting to start a new job. Our office moves fairly quickly and constantly present the best candidates to be interviewed.
Quality Engineer - Chicago, IL
This is for a fast growing organization that is developing novel devices in the spinal sector.
They are seeking a highly motivated Quality Engineer to work in a fast-paced environment that fosters teamwork, change, risk-based decision-making and flexibility. The Quality Engineer will support all new spine implants & instruments development activities and associated manufacturing processes and will actively participate in continuous improvement and support activities of existing products. This individual will develop risk assessment, inspection methodology and acceptance criteria for inspection sample plans and conduct audits of new suppliers as part of the project teams. The Quality Engineer will be able to communicate effectively at all levels within Quality as well as cross functionally with departments such as R&D, Regulatory, Operations & Manufacturing, and Marketing.
Sr. Product Development Engineer - Shelton, CT
This is for a growing stable privately held spine company that focuses on developing unique spinal implants and instruments.
This is a great opportunity for an experienced engineer to develop the next generation of products. This position is highly visible. It reports to a Dir of Engineering, but it will interact with the company’s CEO and CTO as well as the various department heads.
The candidate will develop products from concept to launch, need to have experience interacting with surgeons, must know how to work in a cross functional role, so project management experience is important.
We are conducting a national search; relocation assistance is being offered.
Senior Engineer -Dallas, TX
This position will have the responsibility of developing orthopedic implants and instruments from concept to launch (CMF and small bone). It involves working with a cross-functional team. interacting with surgeons and various departments within the organization to establish requirements, project costs and resources
I am searching for candidates that are strong with design control and project management. Candidates must have successfully developed products from concept to market to be considered.
Relocation assistance is being offered.
The engineer will ensure that the project is completed in a cost-effective and timely manner. These professionals ensure that project financial budgets are adhered to and projects are completed in the required time frame and that all products are designed & developed to meet regulatory requirements and quality standards.
Currently conducting a search for:
JR & SR level Product Development Engineers (Connecticut) - use your 2-5 year orthopedic/spine experience to develop cutting edge implants and instruments.
JR level Product Development Engineer (San Antonio, TX) - This is for a young fast growing organization that is developing novel devices in the orthopedic sector.
Principle Engineer (Dallas, TX) - will have the responsibility of developing orthopedic implants and instruments from concept to launch.
SR. Product Development Engineer (Fremont, CA) - experience in spinal implants and looking for leadership candidate
Regulatory Affairs Manager (Tempe, AZ) - Work with an Industry leader! Candidate will work with a high level of autonomy to bring medical devices to market.
SR Manager of Regulatory Affairs (Bay area, Ca) - Do you have a successful track record leading, managing and developing regulatory affairs teams?
Principal Regulatory Affairs Specialist (Santa Rosa, CA) - This is for a growing device company that is developing novel products to address aortic diseases.
Quality Assurance Specialist (Cleveland, Ohio) - a Quality Assurance Specialist with 3 or more years of experience in Quality Compliance/Quality Systems . This is for a growing start-up orthopedic device company. This person will be responsible for setting up and maintaining the company’s quality system.
Quality Engineer (Chicago, IL) - a growing spine company looking for experienced candidiate
Regulatory Affair Specialist (Cleveland, Ohio) - with 5 or more years of regulatory submission experience. This is a ground floor opportunity and will be the first full time regulatory affairs professional to join the team.
Regulatory Affair Specialist (Valley, PA) - with 4 to 10 years experience with 510K and Domestic FDA submissions.
Strategic Sourcing Manager (Valley, PA) - Leadership role for a candidate with 10-20 years of experience and knowledgeable in FAP, FDA regulations, worked with non-inventory items and a team player.
Director of Regulatory Affairs (Dallas, TX) - Responsible for development and coordination of all harmonized regulatory requirements. Develops and implements strategies for earliest possible approvals to support business plans.
In process to conduct search:
Manager of Regulatory Affairs (CA) - Position description being finalized.
Product Manager (PA) - Position description being finalized.
JR. , SR. & Associate level Engineer (IL) - 3 Position descriptions being finalized.