- Kelly Services (Irvine, CA)
- …_Ability to communicate effectively, both in writing and verball_ + _Familiarity with quality and regulatory systems including FDA's Quality System ... _for a long-term contract at one of our_ **_Global Medical Device_** _clients, located in_ **_Irvine, CA_** _._ _Our...with clinicians to develop innovative technologies that improve the quality of care for arrhythmia patients worldwide_ _As a… more
- Caldera Medical (Westlake Village, CA)
- …is Caldera Medical ? Caldera Medical is a growth stage medical device company dedicated to improving the quality of life for women. In 2018, Caldera ... Product Manager 100% ONSITE - Westlake Village, California Caldera Medical 's Mission - To Improve the Quality ...a related field (Master's/MBA preferred). * 7+ years of medical device product management with at least… more
- Medtronic (Northridge, CA)
- …management framework, ensuring compliance with ISO 10993 standards and global medical device regulations. This role involves conducting comprehensive ... related fields. MS or PhD preferred. + Strong understanding of ISO 10993 and global medical device regulations (eg, EU MDR, FDA, REACH, Prop 65). + Experience… more
- Globus Medical, Inc. (San Diego, CA)
- …+ Minimum five years of mechanical design engineering experience, preferably in the medical device field + Bachelor's degree in Mechanical Engineering or similar ... At Globus Medical , we move with a sense of urgency...of tasks while remaining in full compliance with Globus quality system and other applicable regulatory bodies… 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...Requirements:** Bachelor's Degree with 7+ years of experience in Quality and/or Regulatory , including direct experience in… more
- Gilead Sciences, Inc. (Foster City, CA)
- …communication skills are required. + Demonstrated ability to facilitate the interface with medical device vendors and HF consulting firms. + Demonstrated ability ... aspirations. Join Gilead and help create possible, together. **Job Description** The Device , Packaging and Process (DPP) function is a key component of Gilead's… more
- Globus Medical, Inc. (Redwood City, CA)
- …3 years with a PhD - related experience with development or verification in the medical device industry. (class III medical device experience preferred). ... At Globus Medical , we move with a sense of urgency...and reports, and validation plans and reports. Works with Quality and Regulatory Engineers for the release… more
- Veterans Affairs, Veterans Health Administration (Long Beach, CA)
- …Report: Not required Preferred Experience: Specialized expertise in areas such as Medical Device Isolation Architecture (MDIA) and Specialized Device ... basis with limited oversight by senior biomedical engineers. They participate in medical device hazard investigations, to assure compliance with patient safety… more
- Actalent (Santa Clara, CA)
- …oversight on proper documentation for regulatory submissions. Essential Skills + Medical device experience and understanding of an ISO13485 environment. + ... it into clear documentation for internal and external use in a medical device environment. Responsibilities + Distill technical information into accessible… more
- Kelly Services (Irvine, CA)
- …Johnson & Johnson is rapidly expanding and is immediately hiring qualified R&D Medical Device Technician to support production demand and new product ... development. **Position Summary:** As an R&D Medical Device Technician you will play a...moderately complex processes/product tests and audits for conformity to quality and/or regulatory requirements. + Performs self-inspections… more