- Caldera Medical (Westlake Village, CA)
- …and provide regulatory input and guidance to cross-functional partners regulatory documentation for medical device approvals in compliance with EU MDR, ... your role as a Sr. Regulatory specialist, you will develop and implement medical device regulatory strategies to obtain timely approvals from worldwide… more
- Hologic (San Diego, CA)
- …practices, particularly in Breast/GYN or General Surgery. + Strong knowledge of medical device regulations, compliance standards, and risk management ... Sr Director, Medical Safety Officer San Diego, CA, United States...dynamic and fast-paced environment. + Ethical and professional, ensuring compliance with regulatory and legal standards. + Innovative and… more
- J&J Family of Companies (Santa Clara, CA)
- …Director or above in a quality function across Design and Development including End-to-End Quality & Compliance in Medical Device . + Must have a minimum of 5 ... of Companies, is recruiting for Head of Quality and Compliance (Q&C) Leader for our Monarch platform. This role...regulated industry with at least 12 years in a medical device industry. + A minimum of… more
- Oura (San Francisco, CA)
- …Regulation (QSR) and Good Manufacturing Practices (GMPs), as well as post-market compliance , including Medical Device Reporting (MDR), product recalls, ... local co-working locations. The AGC, Senior Director of Regulatory Compliance & Privacy will provide strategic legal guidance on...wearable devices and related software, including Software as a Medical Device (SaMD), Software in a … more
- Fujifilm (Sacramento, CA)
- …to be an integral part of the legal team providing support to the Medical Device businesses of FUJIFILM Healthcare Americas Corporation and FUJIFILM SonoSite, ... responsible for working independently and collaboratively on legal issues affecting the Medical Device businesses to minimize risks of legal liability and… more
- Mallinckrodt Pharmaceuticals (Sacramento, CA)
- …and documented in compliance with the company quality system and medical device regulations. Innovation Environment: Work with the latest medical ... Job Title Senior Technical Product Specialist - Medical Device Requisition JR000015165 Senior Technical Product Specialist - Medical Device (Open)… more
- IQVIA (San Bernardino, CA)
- …Sales Consultants_** to join our team of field employee's. **Associate Sales Consultant - Medical Device ** If you have ever wondered about the intricacies of ... surgical procedures or considered a career path in medical device sales, this is the role...and maintain the highest levels of professionalism, ethics and compliance at all times. + Analyze product performance and… more
- AbbVie (Irvine, CA)
- …CFR Parts 3, 4, GCP, GLP, 210/211, 820 QSR (Design Control), European Medical Device Directives and Regulation (MDR/IVDR), ISO 13485, MDSAP, technical standards, ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...compliance trends to drive proactive initiatives to ensure compliance for Device /Combination Products. + Understanding of… more
- Kelly Services (Irvine, CA)
- …CA. Johnson & Johnson is rapidly expanding and is immediately hiring qualified Medical Device Assemblers to support production demand and new product ... development. **Position Summary:** As a Medical Device Assembler, you will play a...of new products onto the manufacturing line. + Maintain compliance with GMP, ISO, SOP, and safety guidelines. +… more
- AbbVie (Pleasanton, CA)
- …Must have 1 year of quality engineering work experience in FDA regulated medical device manufacturing environment(s). If experience required, must have 1 year ... drawings & GD&T + performing daily assigned tasks in compliance with FDA's Quality System Regulation (QSR), ISO 13485,...MDR, & MDSAP; + performing all tasks according to medical device development life cycles, manufacturing processes… more