- Abbott (St. Paul, MN)
- …+ HS Diploma or equivalent + Minimum 2 years' experience in related field + Medical device experience + Tissue sewing experience **Learn more about our health ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Actalent (Plymouth, MN)
- …HPLC, GC, dissolution Method development experience Method validation experience Pharmaceutical or Medical Device experience Pay and Benefits The pay range for ... * Develops robust methods that are time tested in a routine quality control environment. Leads method troubleshooting and rectifies challenges effectively using a… more
- J&J Family of Companies (New Brighton, MN)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... School diploma or GED or 0-2 years' in a medical device environment or equivalent experience in...work environment. + Knowledge of and compliance with applicable Quality System requirements such as QSRs, FDA ,… more
- ManpowerGroup (Plymouth, MN)
- Our client, a leader in the medical device industry, is seeking a Senior Engineer to join their team. As a Senior Engineer, you will be part of the engineering ... and manage supplier relations effectively. + Ensure compliance with FDA regulations and ISO 13485 Quality Management...Single Use Disposable Experience highly preferred. + Experience with medical device design outputs and change control… more
- Medtronic (Minneapolis, MN)
- …Methods for a new Product Development project for a complex electro-mechanical medical device . Candidate should have experience leading teams and ... not essential + Practical knowledge of project management. + Medical Device Industry experience. + Familiarity with...Device Industry experience. + Familiarity with these regulations: FDA 21 CFR Part 820 cGMP, ISO 13485, ISO… more
- Abbott (Plymouth, MN)
- …Degree within Technical or business field, preferred + Minimum 10 years + Medical device development and/or other highly regulated industry. + Experience working ... the Structural Heart Division. Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions… more
- Medtronic (Fridley, MN)
- …cross-functionally. + Experience with Inductive Automation Ignition (Perspective). + Experience in FDA -regulated industries such as medical device or ... ensuring systems meet both technical specifications and regulatory standards (eg, FDA , 21 CFR Part 11). You'll work closely with cross-functional engineering,… more
- Abbott (Plymouth, MN)
- …2-5 years of engineering experience, preferably in Research & Development engineering in medical device or other highly regulated industry/ Master's degree may ... Mission: Why We Exist. Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions for… more
- Fujifilm (St. Paul, MN)
- …United States. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... with a Master's degree. + Minimum 8 years of medical device industry experience in a clinical...evolving situations and needs + Strong commitment to delivering high- quality work and upholding HCUS values. + Proficiency in… more
- Insight Global (Maple Grove, MN)
- Job Description Insight Global is seeking a Principal Systems Engineer for a Medical Device company located in Minneapolis. As a Systems Engineer, your primary ... advantage. . At least five years of experience is required, preferably in the medical device industry, focusing on systems engineering. . Familiarity with system… more