DEKA Research & Development

BS in Engineering, Life Sciences, or related field, 3+ years of experience in quality systems role, working knowledge of FDA QSR and ISO 13485

Bachelor's degree with 1 year of supplier management experience or 5 years of supplier management experience, project coordination and/or project management experience, experience working in an engineering or technical environment

B.S. in Mechanical/Manufacturing Engineering w/2-5 yrs exp. A.S. with 3-6 yrs exp. Strong electromechanical/manufacturing exp. CAD/SolidWorks proficiency is a plus

Bachelor's in engineering or related field. 3+ yrs industrial vision experience. Proficiency in Python or Keyence vision systems. Requires on-site work.

Associate’s degree or equivalent experience. 5+ years in mechanical or electro-mechanical production. Must be able to learn and troubleshoot electronics, mechanical device assembly, and manual work

5-8 years machining exp, CAD/CAM proficiency, and experience with Machining machines & measuring equipment are key. Blueprint reading and clean work environment skills are also important

Bachelor’s degree in biomedical engineering or related field; 2-4 years cGMP experience; or 2-year degree + 5 years cGMP experience. Strong skills in problem-solving & communication required

Bachelor's degree in engineering, 5+ years leading product development teams, experience with medical device development and project management

1+ year technical school completed. 1+ year machining experience. Basic understanding of blueprint reading

4+ yrs PCB/EE design experience. Proficient in Altium. Knowledge of signal integrity, EMC, and manufacturing processes. Strong communication and problem-solving skills are vital