- Abbott (Alameda, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... levels with our new sensing technology. **The Opportunity** This ** Regulatory Affairs Manager** will work on-site in Alameda, CA...submissions (PMA, IDE, 510(k)) for Class II, and III medical devices or EU Technical Files or… more
- J&J Family of Companies (Irvine, CA)
- …in providing therapeutic and clinical expertise in support of the development of medical devices for the treatment of structural heart diseases. This position ... experience leading Medical /Clinical teams in a regulated, commercial biomedical or medical device business is strongly preferred. + Experience in product… more
- Actalent (Minneapolis, MN)
- …Illustrator, Adobe Photoshop, and document management systems is a plus. + Knowledge of regulatory affairs and medical device labeling. + Graphic design and ... 3-5 years of experience in technical writing or technical communications within the medical device industry. + Proficiency in Adobe InDesign and Microsoft Office… more
- Abbott (Sylmar, CA)
- …of statistics to health care + Understanding of the US and International regulatory environment for medical device development, manufacturing, and ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- J&J Family of Companies (Cincinnati, OH)
- …environments and participating in the creation of user workflows + Understand the regulatory imperative for medical device human factors, including relevant ... journey to wellness. Learn more at https://www.jnj.com/medtech The Johnson & Johnson Medical Devices (JJMDC) Industrial Design and Human Factors (IDHF)… more
- Knowles Precision Devices (Liberty, SC)
- …Safety (EHS) Manager. This role is critical for ensuring compliance with regulatory standards and maintaining a safe, healthy work environment across multiple ... Develop, implement, and monitor EHS policies, procedures, and programs to ensure regulatory compliance and a safe work environment across multiple facilities. + Lead… more
- Teleflex (Morrisville, NC)
- …in a regulated environment is required. * Basic understanding of, or experience with, medical devices with electrical capabilities is a plus. * Regulatory ... Regulatory Affairs Specialist **Date:** Sep 9, 2025 **Location:**...with 2-3 years of overall class I or II medical devices , is highly preferred. **Specialized Skills… more
- Integra LifeSciences (Plainsboro, NJ)
- …Expertise in one or more of the following areas: + Manufacturing of medical devices , pharmaceutical API, or drug products, Facilities, Engineering, Laboratories, ... + Strong knowledge of auditing techniques. + Minimum of 3-5 years of Medical Device , Pharmaceutical or related experience, preferably in FDA regulated industry.… more
- Stryker (Tempe, AZ)
- …for serious or life-threatening medical conditions or that address unmet medical needs + Leads negotiations with regulatory and other health authorities ... regulatory compliance requirements for changes affecting product submission and device manufacturing in global markets + Implement regulatory system changes… more
- Abbott (Santa Clara, CA)
- …meet the existing and emerging regulatory requirements, particularly the EU Medical Device Regulations (EU MDR) and ISO 10993 series. **Principal ... of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines....Biocompatibility support to the research & development of new medical device products as well as the… more