- Merck & Co. (Rahway, NJ)
- …authoring ISO-13485 and 21 CFR 820 compliance technical documents, design controls, device risk management, medical device , combination products, prefilled ... sites, External Manufacturing, R&D, Quality, Operations, Product Development groups, Regulatory Affairs , Procurement, and suppliers. Key Functions Work… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …biotechnology industry experience (including roles in research and development (R&D), clinical trials, regulatory affairs , or medical affairs Leadership ... of a drug development function such as Clinical Drug Development (preferred) or Medical Affairs . Experience managing teams and large-scale projects is essential… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …non-clinical research, translational biomarkers, companion diagnostics, bioinformatics, clinical development, medical affairs , regulatory etc.).Identify and ... he or she will interact with the Companion Diagnostics Lead, Non-Clinical Research, Medical Affairs and other stakeholders to support the program. Other… more
- Merck & Co. (Washington, DC)
- …healthcare, commercial trade, regulatory , or intellectual property-Pharmaceutical sector, medical device , or related policy background preferred with ... policy professional with at least 10 years' experience in international government affairs roles in governments, think tanks or business associations responsible for… more
- Merck & Co. (Washington, DC)
- …drive policy change at local, regional, and global levels. Pharmaceutical sector, medical device , or related policy background preferred with specific emphasis ... policy professional with at least 10 years' experience in international government affairs with a preference for candidates with experience in government, think… more
- Merck & Co. (Rahway, NJ)
- … regulatory , or intellectual property. Government experience preferred.-Pharmaceutical sector, medical device , or related policy background preferred with ... professional with at least 15 years' experience in international government affairs in governments, think tanks or business associations responsible for healthcare,… more
- Merck & Co. (Washington, DC)
- …commercial trade, regulatory , or intellectual property Pharmaceutical sector, medical device , or related policy background preferred. Experience in ... policy professional with at least 5 years' experience in international government affairs roles in governments, think tanks, or business associations responsible for… more
- Exact Sciences (Boston, MA)
- …collaboration with a range of internal stakeholders including Screening Advocate (SA), Medical Affairs and Marketing. Inform, educate and enable target physician ... fight against cancer. The SSS will drive product growth of Cologuard in medical practices to meet sales goals within the assigned geography and deliver diagnostic… more
- Arthrex (Naples, FL)
- Arthrex, Inc. is a global medical device company and a leader in new product development and medical education. We are a privately held company that strives ... other status protected by law.Arthrex, Inc. is a global medical device company and a leader in...making. Provide support to Engineering Teams, Legal, Quality Assurance, Regulatory Affairs , Product Management, Sterilization, and Marketing… more
- Dunhill Professional Search (Rapid City, SD)
- …procedures, planned maintenance, and repair service on various types of medical equipment.Understanding of regulatory agencies' requirements, industry ... several Biomedical Technicians to support the Department of Veterans Affairs as they roll out a new Electronic Health...inspection and periodic inspection on both new and current medical equipment or devices andPerform quality assurance check to… more
- Abbott (Santa Clara, CA)
- …with diabetes from routine fingersticks. We currently have several opportunities for the ** Medical Device Regulatory Affairs Development (RAD) Program** ... CA, Minneapolis, MN or Plano, TX. This position is included in the ** Medical Device Regulatory Affairs Development (RAD) Program** and performs three… more
- Medtronic (Minneapolis, MN)
- …with a minimum of 5 years of relevant experience + Or minimum 5 years of medical device regulatory affairs experience with Master's degree **Preferred ... Class III medical devices. The Sr Principal Regulatory Affairs Specialist is responsible for activities...experience:** + 4+ years of medical device industry experience with US FDA… more
- Medtronic (Plymouth, MN)
- …medical , or vigilance. **Nice to Have** + Bachelor's degree with 2+ years of medical device regulatory affairs experience + Interpersonal, analytical, ... in a more connected, compassionate world. **A Day in the Life** The Regulatory Affairs Specialist (RAS) is responsible for collaborating, planning and executing… more
- Philips (Chicago, IL)
- …right fit if:** + You've acquired a minimum of 7 years' experience in FDA regulated Medical Device Regulatory Affairs , with proven expertise in US FDA ... The Principal Regulatory Affairs Specialist will play a...devices globally. + You have experience with Software as Medical Device (SaMD), and Ultrasound Imaging Devices… more
- Teleflex (Morrisville, NC)
- …experience may be acceptable in lieu of a degree. * 7 to 10 years of related Medical Device Regulatory Affairs with experience in Class I and II ... Sr. Regulatory Affairs Manager - Product Management...directly to the company's growth and reputation within the medical device industry. **Principal Responsibilities** 1. Oversee… more
- Stryker (San Jose, CA)
- …an FDA regulated environment required + Minimum 4 years of full-time work experience in medical device regulatory affairs required + Demonstrated applied ... benefits. (https://d25zu39ynyitwy.cloudfront.net/oms/000000/document/2024/6/SMVZW\_USStrykerEmployeebenefits/USStrykerEmployeebenefits.pdf) We are currently seeking a **Senior Staff Regulatory Affairs Specialist** to join our Endoscopy… more
- Bristol Myers Squibb (Princeton, NJ)
- …BSN, etc.) with 5 years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in ... careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion… more
- Abbott (Atlanta, GA)
- …business unit model. + Experience working in the Medical Device industry. + Regulatory Affairs Professionals Society Certification ... place to work for diversity, working mothers, female executives, and scientists This ** Regulatory Affairs Specialist II** will work on-site out of our Atlanta,… more
- Bausch + Lomb (Bridgewater, NJ)
- …deadlines. + Other duties as assigned. **Requirements** **TECHNICAL COMPETENCIES:** Knowledge of medical device regulatory affairs discipline throughout ... regulations. + Leads meetings and discussions with cross-functional teams ( Regulatory Affairs , Medical Affairs...relating to submissions and regulatory approval of medical devices. Knowledge of medical device… more
- Zimmer Biomet (Warsaw, IN)
- …FDA/EU + A minimum of 3 years of experience in orthopaedic or medical device industry preferred + Regulatory Affairs Certification (US or EU) preferred + ... innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's...modified products. Interprets results of research + May assign regulatory affairs (RA) professionals to serve on… more
