Diversatek, Inc. is a global, multi-platform healthcare solutions manufacturing company. Invested in a broad and ever-growing line of medical technologies, Diversatek manufactures and markets products and solutions for diagnostic and therapeutic gastroenterology procedures, continuing care and rehabilitation, and medical device OEMs. Diversatek owns and operates manufacturing facilities in Wisconsin, Colorado, Brazil, and Vietnam. Our Technical Research and Training Center in Highlands Ranch, Colorado, boasts a best-in-class clinical education and product training center for healthcare providers worldwide.
Are you an engineer who thrives on solving complex problems in the medical device industry? Do you often find you are most successful in a work environment that challenges your strong intellectual curiosity? We have an exciting opportunity for an Electrical Engineer who is looking to exercise their problem solving and intellectual curiosity. The successful candidate will participate in the development of products throughout the entire cycle, from inception to technical design, and through commercialization.
- Design, develop, test, and support hardware and firmware for next-generation medical diagnostic products.
-
Provide engineering production support for existing medical diagnostic product lines.
-
Troubleshoot complex production and field issues, perform root cause analysis, and implement corrective actions.
-
Lead or support product verification and validation activities required to qualify and release medical diagnostic devices.
-
Lead the transition from engineering development to production, including creation of design documentation, test procedures, and production fixturing.
-
Develop and support automated production test hardware and software.
-
Collaborate cross-functionally with manufacturing, quality, regulatory, and other engineering teams to ensure continuity of design and requirements.
-
Perform failure analysis investigations and recommend design or process improvements
-
Ensure product development and sustaining activities comply with IEC, FDA, CE, MDSAP, ISO, and other requirements.
-
Create and maintain technical documentation including schematics, drawings, specifications, test protocols, risk management files, engineering change orders, and regulatory submissions.
-
Perform other engineering-related tasks as required.
