- Medtronic (Lafayette, CO)
- …+ Maintain up-to-date knowledge of cybersecurity regulations and standards specific to the medical device industry (FDA, HIPAA, IEC 62443, NIST, NIS 2, etc.). ... Risk, & Compliance), or external/internal audit, preferably within the medical device or healthcare industry. + Strong...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Medtronic (Santa Rosa, CA)
- …discipline + Minimum of 7 years of direct Regulatory Affairs experience within the medical device or other regulated industry, + Or advanced degree with a ... minimum of 5 years of Regulatory Affairs experience. + Medical device industry experience with Class I/II/III/IV...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Medtronic (Santa Rosa, CA)
- …applicant profile_ + Bachelor's degree in a technical discipline + Minimum 4 years of medical device regulatory experience + Or minimum 2 years of medical ... + In depth experience with FDA requirements, guidance documents, Medical Device Regulation, ISO 14971, ISO 13485,...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Medtronic (Los Angeles, CA)
- …and high-quality work. + Understand the various regulations we operate under in the medical device industry and ensure that the statistical methods applied align ... MS or PhD degree in Statistics or equivalent + Medical device domain knowledge Experience with Diabetes...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Medtronic (Mounds View, MN)
- …and secure by design development focus * Experience creating design and release documentation for medical device or non- medical device product releases * ... aspects of the company's design and development of new medical device products or software systems. +...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Medtronic (Tempe, AZ)
- …a workplace environment that reflects Medtronic's standing as the world's top medical device company. Help us engineer the extraordinary! Do meaningful ... + Ability to inspire, train, facilitate, and lead. + Medical device manufacturing and operations experience. +...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Medtronic (Santa Clara, CA)
- …Life Sciences, or related field with minimum 4 years of quality systems experience in medical device industry + Strong knowledge of medical device ... Senior Quality Systems Specialist to develop and maintain quality programs for medical devices. The role ensures compliance with regulatory standards and supports… more
- Medtronic (Los Angeles, CA)
- …our technology transforms lives Ensure complete and accurate maintenance and reporting of Medical Device Reports (MDRs), Adverse Drug Experience (ADE) data or ... to meet goals and objectives. Understand current and upcoming Medical Device Reporting (MDRs) and EU Vigilance...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Medtronic (Pittsburgh, PA)
- …+ Strong understanding of regulatory requirements and industry standards governing medical device reprocessing. + Excellent communication, interpersonal, and ... instrumentation. Commitment to upholding the highest standards of safety and quality in medical device reprocessing. + This position is in the east coast… more
- Medtronic (Tempe, AZ)
- …on creating a workplace environment which reflects our standing as the world's top medical device company. The ideal candidate will have a passion for the ... and materials + Document and approve acceptance record as part of the Device History Record(s) + Review lot history documentation for discrepancies or missing… more