- Abbott (Lake Forest, IL)
- …working mothers, female executives, and scientists. **The Opportunity** The position of Regulatory Specialist II is within our Toxicology business. ... colleagues serve people in more than 160 countries. **_Regulatory Affairs Specialist II_** **Working at Abbott** At...this role, you will work as part of the Regulatory Affairs department with direct responsibility for… more
- Zimmer Biomet (Broomfield, CO)
- …cared for, valued, and have a strong sense of belonging. **What You Can Expect** The Regulatory Affairs Specialist II collaborates with the Regulatory ... duties as assigned **What Makes You Stand Out** A Regulatory Affairs Specialist can stand...Devices + Familiarity with Device Classifications: Knowledge of Class II and III orthopedic devices (eg, implants, surgical instruments,… more
- Abbott (St. Paul, MN)
- …a best place to work for diversity, working mothers, female executives, and scientists This ** Regulatory Affairs Specialist II ** will work on-site at our ... + Experience working in the Medical Device industry. + Regulatory Affairs Professionals Society Certification is a...in the Medical Device industry. + Regulatory Affairs Professionals Society Certification is a plus. Apply Now… more
- Abbott (St. Paul, MN)
- …for the treatment of structural heart disease. The Opportunity - We are seeking a Regulatory Operations Specialist I for our St. Paul, MN Structural Heart team ... work assignments and/or analyses, evaluation, preparation and general support of global regulatory activities. What You'll Work On - * Assists in the preparation… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …position to act as a team member in the product manager area of Regulatory Affairs (Biopharma) supporting global submissions for various areas of the business. ... to support business needs in a very timely and accurate manner. **_Sr Reg Affairs Specialist I_** **Primary responsibilities for role:** + Act as Regulatory… more
- Medtronic (CO)
- …innovation in a more connected, compassionate world. **A Day in the Life** The Principal Regulatory Affairs Specialist will have a role in supporting product ... devices across the cranial and spine space. The Principal Regulatory Affairs Specialist will be...in submission ready outputs. + Develop and support global regulatory strategies for Class I, II , and… more
- Stryker (Redmond, WA)
- We are currently seeking a **Senior Regulatory Affairs Specialist ** to join our **Medical** **Division** to be based **Hybrid** in **Redmond, Washington.** ... certification or Advanced Degree (Masters in Regulatory Affairs ). + Previous experience with Class II /III... Affairs ). + Previous experience with Class II /III medical devices. + Experience authoring regulatory … more
- Teleflex (Chelmsford, MA)
- Sr. Regulatory Affairs Specialist **Date:**...and international. 3 years of experience with Class I, II or III medical devices. * Proven history of ... that make a difference in patients' lives. **Position Summary** The Sr. Regulatory Affairs Specialist (SRA) will develop US, EU, and Canada strategies,… more
- Abbott (St. Paul, MN)
- …female executives, and scientists **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist ** to join Abbott's Vascular Division ... vascular disease. As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to...Class II and/or Class III medical devices. Regulatory Affairs Certification (RAC) is a plus.… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …your best self. Become a **maker of possible** with us. **Overview** As Staff Specialist , Regulatory Affairs , you will develop and implement medical device ... from worldwide regulatory bodies. Working with global Regulatory Affairs colleagues, you will ensure submissions...will have primary RA responsibility for multiple FDA Class II products, working within a collaborative team environment that… more
- Stryker (Redmond, WA)
- We are currently seeking a ** Regulatory Affairs Specialist ** to join our **Medical Division** , **Hybrid** , to be based in **Redmond, Washington** . **What ... field + 0-2 years in a Regulatory Affairs role + Previous experience with Class II /III medical devices **Preferred** + Experience authoring regulatory … more
- Terumo Neuro (Aliso Viejo, CA)
- **12814BR** **Title:** Sr. Specialist , Regulatory Affairs **Job Description:** Responsible for preparing strategy for worldwide product approval submission ... writing skills as evidenced by successful US FDA Class II / III medical device submissions, EU CE Mark...to comprehend technical documents and concepts. **External-Facing Title:** Sr Specialist , Regulatory Affairs **Posting Country:**… more
- Globus Medical, Inc. (Audubon, PA)
- …can resume their lives as quickly as possible. **Position Summary** **:** The Lead Regulatory Affairs Specialist oversees the preparation and submission of ... to the Food and Drug Administration (FDA) for class II and class III products. This position entails development...study data with Clinical Data Manager and other Clinical Affairs personnel, as needed for IDE and PMA reporting… more
- Abbott (Alameda, CA)
- …working with Class II , Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification (RAC) is a plus. . Experience with 510(k) ... glucose levels with our new sensing technology. The Opportunity The Principal RA Specialist -Business Partnerships will work on-site out of our Alameda, CA location… more
- Abbott (Alameda, CA)
- …working with Class II , Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification (RAC) is a plus. + Experience with either ... glucose levels with our new sensing technology. **The Opportunity** The **Principal RA Specialist - US New Product Introduction** will work on-site out of our… more
- Edwards Lifesciences (Irvine, CA)
- …difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex ... 5 years related experience; including but not limited to providing regulatory expertise in US PMA Class II and/or Class III products, EU MDR, and working on… more
- Edwards Lifesciences (Irvine, CA)
- …difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex ... domestic and international regulatory environments. Working in...understanding of global regulations relevant to medical devices, Class II and/or Class III devices + Solid knowledge and… more
- Edwards Lifesciences (Irvine, CA)
- …difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex ... domestic and international regulatory environments. Working in...understanding of global regulations relevant to medical devices, Class II and/or Class III devices + Full knowledge and… more
- Edwards Lifesciences (Irvine, CA)
- …more about BD at bd.com **How you'll make an impact:** + Represent the regulatory function on manufacturing and product development teams to provide input on ... regulatory requirements, including presenting alternatives for meeting ...understanding of global regulations relevant to medical devices, Class II and/or Class III devices + Full knowledge and… more
- MyFlorida (Tallahassee, FL)
- REGULATORY SPECIALIST II - 79011169 Date: Apr 29, 2025 The State Personnel System is an E-Verify employer. For more information click on our E-Verify Website ... . Requisition No: 852049 Agency: Business and Professional Regulations Working Title: REGULATORY SPECIALIST II - 79011169 Pay Plan: Career… more