Collaboratively lead medical device development program of small to medium scope, or subsection of large program, from design to production.
Bachelors or foreign equivalent in Biomedical Engineering or in a related biotech or engineering field of study with minimum 5 years of related progressive professional medical device engineering, pharmaceutical engineering, or healthcare engineering experience. Alternatively will accept Masters with minimum 3 years of professional medical device engineering, pharmaceutical engineering or healthcare engineering experience. Each alternative requirement must possess experience in: (i) leading medical device development program of small to medium scope or subsection of large program from design to production through biomedical engineering project management or medical device product development; (ii) developing comprehensive program plans identifying objectives, strategy, risks/risk mitigation, budget, effort estimates & schedule for new medical device product development; (iii) ensuring robust design verification, testing & validation & establishing & contributing to program & product DHF in compliance with company procedures & domestic & international medical device manufacturing regulations including ISO 13485, ASTM, EU MDR & FDA 21 CFR 820; & (iv) utilizing tools & technologies including enterprise resource & project management tools including SAP, MS Project &/or Windchill PLM; CAD software including CREO, AutoCAD or SolidWorks; Minitab statistics & data analysis tool; & visualization tools & technologies, including Gantt Charts.
Employer will accept any suitable combination of education, training, or experience. An EOE. 40 hours/week. $156,270 - $228,000/year. Send resumes to [email protected] or by mail to Abbott Laboratories, Attn: 26J14A, Willis Tower, 233 S. Wacker Dr., Floor 26, Dept. 32, Chicago, IL 60606. Refer to ad code: ABT-0137-ES.
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