- BD (Becton, Dickinson and Company) (Irvine, CA)
- …and critical thinking skills + Full knowledge and understanding of global regulations relevant to medical devices , Class II and/or Class III devices + Full ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...solutions. This role supports the Sustaining activities for disposable devices used with monitoring systems. **How you'll make an… more
- Medtronic (Minneapolis, MN)
- …+ Knowledge and apply this knowledge to post market surveillance of products. + Medical device experience; or experience in a regulated environment + Experience ... expectations of Regulatory Bodies. This is a scientific (engineering, technical, medical ) writing position. This individual will partner with other teams such as… more
- Hussmann Corporation (Bridgeton, MO)
- …+ Ensure engineering work complies with relevant industry standards and regulatory requirements. **Qualifications** + Bachelor's or Master's degree in Systems ... status, disability, age, race, color, religion, sex, national origin, genetics, medical condition, or any other characteristic protected by law. \#LI-SM1 REQ-152634 more
- Amazon (Sunnyvale, CA)
- …- Knowledge of internet, software, and media industries and the legal and regulatory environment in which they operate or equivalent - Experience working closely ... total compensation package, in addition to a full range of medical , financial, and/or other benefits. For more information, please visit… more
- ManpowerGroup (Deerfield, IL)
- …preferred. + Minimum of three months of related experience, ideally in a medical device , manufacturing, or regulatory environment. + Proficiency with ... team. As a Patch Intake Specialist, you will be part of the Medical Equipment Production department supporting the quality assurance and operational goals of the… more
- ThermoFisher Scientific (Rochester, NY)
- …least 2 years of experience in a regulated industry (pharmaceutical or medical device ). **Preferred Qualifications** + Familiarity with product stewardship, ... regulations (EU REACH, CA Prop 65, TSCA). + Understanding of pharmaceutical and medical device standards and regulations (USP, ISO 10993, ISO 13485, IVDR,… more
- Bristol Myers Squibb (Madison, NJ)
- …objectives + Work as part of cross-functional teams-including clinical development, medical affairs, regulatory , and biostatistics-to ensure HEOR contributions ... including data model specifications, project plans, user acceptance testing scripts, device screenshots, site user guides and training slides, and data migration… more
- Edwards Lifesciences (Irvine, CA)
- …and critical thinking skills + Full knowledge and understanding of global regulations relevant to medical devices , Class II and/or Class III devices + Full ... difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and… more
- Globus Medical, Inc. (Audubon, PA)
- …engineering, process improvement, or manufacturing operations. + Strong understanding of medical device manufacturing, regulatory compliance, and quality ... Assurance** + Ensure all Globus products and processes meet regulatory and internal quality standards. + Review, improve, and...and fast-paced team dedicated to innovation and efficiency in medical device development. + Make a meaningful… more
- Family Dollar (Chesapeake, VA)
- …. Oversee the regulatory notification process (eg, market actions such as Medical Device Reports). . Monitor and document product recalls. . Administer and ... Deviation Investigations, recording/tracking/writing Change Controls, writing reports, assisting with Medical Device Reports, assisting with recalls, writing and… more