- Meta (New York, NY)
- **Summary:** We're seeking a regulatory affairs specialist to join our medical devices compliance team. You will get to work on wearables and Software as ... wearables, and other innovative devices . **Required Skills:** Medical Devices , Regulatory Specialist...work experience 6. 3+ years of industry experience in medical device regulatory affairs or… more
- Meta (New York, NY)
- …with distribution into many worldwide markets. **Required Skills:** Medical Devices Regulatory Affairs Strategy Specialist Responsibilities: 1. Act ... form factors can do. We are seeking an experienced medical devices regulatory affairs professional...Medical Device Directive & European Union Medical Device Regulation, FDA regulatory … more
- Canon USA & Affiliates (Trenton, NJ)
- ** Regulatory Affairs Specialist - Post Market -...Word, Excel, Oracle, Sales Force, etc. + 2 Years Regulatory Affairs experience in medical device ... req1434** **OVERVIEW** Reporting to the Director Regulatory Affairs, the Regulatory Affairs ...$72,000 to max $116,100 (annual equivalency) **_About us!_** _Canon Medical Systems USA, Inc., a world leader in diagnostic… more
- Edwards Lifesciences (New York, NY)
- …**_Note: this Clinical Specialist will support field cases for EVOQUE (tricuspid device ) in the local region, along coverage when needed in the broader US_** ... the world. As a part of the Field Clinical Specialist team, you will be a critical part of...you will make an impact:** + Educate physicians on device handling, implantation and troubleshooting techniques related to the… more
- Rep-Lite (Manhattan, NY)
- …to implantable or neuromodulation devices + Previous experience supporting medical device or pharmaceutical products + Ability to communicate effectively ... Associate Clinical Specialist - Neuromodulation Full-Time | Field-Based | Travel...This role is ideal for individuals early in their medical device career who want to grow… more
- Eurofins (North Brunswick Township, NJ)
- …in Quality Assurance within a laboratory or regulated industry (eg, pharmaceuticals, biotechnology, medical devices ). + Must have experience working in a GMP ... ISO, GLP, GMP) + Experience with testing of pharmaceutical, cosmetic, and/or medical device products. Capabilities: + Must be a detail-oriented, self-initiating… more
- Intermountain Health (Trenton, NJ)
- **Job Description:** The CE Medical Equipment Technology Specialist is responsible for providing analysis and support for the development of standardized ... standards using continuous improvement principles. + Intermediate knowledge of regulatory requirements pertaining to medical equipment management. **Skills**… more
- Cardinal Health (Trenton, NJ)
- …operating procedures for supplier qualifications including, but not limited to drugs, medical devices , and dietary supplements. + Demonstrates an understanding ... procedures, and processes to ensure products and services comply with regulatory standards and specifications. Quality Assurance develops and implements a compliant… more
- Fujifilm (Trenton, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... **Position Overview** The Specialist , Clinical Applications - MR position is responsible...needs associated with training others on the operation of medical imaging equipment and conveying to the Fujifilm organization… more
- Astrix Technology (New Brunswick, NJ)
- …critical documentation and testing per procedures to ensure high-quality, safe material and medical devices . + Approve release of processed material or ... **Quality Specialist ** Quality Assurance Middlesex County, NJ, US Pay Rate...medical devices for use, ensuring all non-conformances are resolved. + Review… more
- Fujifilm (Trenton, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... **Position Overview** The Sales Specialist , Diagnostic Oncology, in the Invitro Diagnostics Division,...with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and… more
- Integra LifeSciences (Princeton, NJ)
- …Computer Science or Software Engineering. + 8+ years of relevant experience in pharmaceutical/ medical device industry. 4-5 years of proven experience in an ... As part of Integra's Business Systems Team, the Quality Systems Senior Specialist is a seasoned professional with complete and in-depth conceptual and practical… more
- Windstream Communications (Trenton, NJ)
- …a world of infinite possibilities! ** ** **About the Role:** The Information Security Specialist is a crucial member of the Threat Detection and Response (TDR) team, ... an analytical mindset to detect, investigate, and mitigate potential security incidents. The Specialist will act as both a subject matter expert and a mentor,… more
- Fujifilm (Trenton, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... + $50,760.00 variable comp opportunity + Company Car + Medical , Dental, Vision + Life Insurance + 401k +...against COVID-19, absent being granted an accommodation due to medical or sincerely held religious belief or other legally… more
- Abbott (New Brunswick, NJ)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... improve people's health. We're always looking towards the future, anticipating changes in medical science and technology. **Working at Abbott** At Abbott, you can do… more
- Evolent (Trenton, NJ)
- …in a non-clinical setting? Join our Utilization Management team as a Field Medical Director, Cardiovascular Specialist and use your expertise in interventional ... cases (eg, cardiac catheterizations, coronary interventions, endovascular procedures, implantable cardiac devices , etc) that do not initially meet medical … more
- Fujifilm (Trenton, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... a key account in the role of a clinical specialist (if the organization is resource constrained). + Partner...with a Master's degree. + Minimum 8 years of medical device industry experience in a clinical… more
- Amazon (New York, NY)
- Description AWS is seeking a Security Assurance Specialist who will drive the strategy that enables every customer, in every sector of the United States. This ... You will have a desire to learn and understand the complexities of legal, regulatory and compliance requirements across all sectors of your region. You will be… more
- NTT America, Inc. (Trenton, NJ)
- …and enforcing the corporate-wide personnel safety, environmental, health and regulatory management programs. This position has the responsibility for ... Health and Safety programs that meet or exceed local, regional, and national regulatory compliance standards, along with NTT corporate value statements. + Provides a… more
- Fujifilm (Trenton, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... **Position Overview** The Digital Radiography Sales Specialist is the regional DR and CT expert...the product sales, product marketing at a Healthcare / Medical Imaging / IT organization. + Broad functional experience… more