- Microsoft Corporation (Redmond, WA)
- …sign‑in, session management, token issuance/validation, service‑to‑service auth, and cross‑ device experiences. + Cross‑surface platform leadership: Drive common ... Product mindset: Balance customer experience with consumer-grade security, privacy, and compliance expectations for Copilot. + Work closely with globally distributed… more
- Jabil (Auburn Hills, MI)
- …experience in Manufacturing Engineering or Quality Engineering. + Experience in medical device manufacturing and regulated environments preferred. Knowledge, ... as a technical liaison between Jabil, suppliers, and customers, ensuring compliance with regulatory standards and driving continuous improvement. Your success in… more
- BD (Becton, Dickinson and Company) (Durham, NC)
- …implementation examples + Experience championing cybersecurity initiatives within regulated medical device environments + Consistent track record supporting ... primary responsibilities are to support new product development activities, maintain compliance to company procedures and external standards, manage design history… more
- Cardinal Health (Indianapolis, IN)
- …210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device ) preferred + Possess an understanding of cGMP/ compliance requirements for cosmetic ... and evaluate their potential impact on product quality and compliance + Champion Quality, GMP compliance and...benefits and programs to support health and well-being. + Medical , dental and vision coverage + Paid time off… more
- GE HealthCare (Waukesha, WI)
- …+ Extensive experience in medical industry + Experience in industry of medical device development and processes + Experience in communicating scientific data ... this job type/position + Complete all planned Quality & Compliance training within the defined deadlines + Identify and...defined deadlines + Identify and report any quality or compliance concerns and take immediate corrective action as required… more
- Envista Holdings Corporation (Brea, CA)
- …Engineering or a related field. + 5 years of experience in quality engineering within medical device industry. + FDA Quality System Regulation Part 820 and ISO ... lifecycle. + Performs quality engineering reviews of design documentation for compliance with stated requirements. + Lead complex technical problems where analysis… more
- HCA Healthcare (Austin, TX)
- …and retirement of our colleagues. The available plans and programs include: + Comprehensive medical coverage that covers many common services at no cost or for a low ... health coverage as well as free telemedicine services and free AirMed medical transportation. + Additional options for dental and vision benefits, life and… more
- BD (Becton, Dickinson and Company) (Canaan, CT)
- …Minimum: High School Diploma/GED **Experience:** + Minimum of 1 year in a medical device manufacturing or similar experience. **Knowledge and Skills:** + Strong ... consistently meet quality system requirements, product standards, and regulatory compliance . This position is responsible for reviewing documentation, releasing… more
- PACIV (Indianapolis, IN)
- …solutions and instrumentation, we serve clients in the life sciences, pharmaceutical, medical device , food & beverage, and utilities sectors, specializing in ... and proactive Validation Engineer II for our Indianapolis, IN office to support compliance and efficiency in a regulated environment. This role is responsible for… more
- Zimmer Biomet (Englewood, CO)
- …in Engineering or technical discipline * 4+ years in related field, preferably medical device or manufacturing * Auditing experience, ISO 13485 preferred * ... pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by… more