- Zimmer Biomet (Fort Collins, CO)
- …and have a strong sense of belonging. **Compensation Data** **What You Can Expect** The Regulatory Affairs Specialist II collaborates with the ... 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
- Actalent (Irvine, CA)
- Regulatory Affairs Specialist II As a Regulatory Affairs Specialist II , you will play an essential role in ensuring compliance with ... develop materials for these meetings. + Essential Skills + Experience in regulatory affairs within the medical device industry. + Proficiency in regulatory … 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
- Abbott (Alameda, CA)
- …place to work for diversity, working mothers, female executives, and scientists This **Senior Regulatory Affairs Specialist ** will work on-site out of our ... technology. **The Opportunity** As an individual contributor, the Senior Regulatory Affairs Specialist will support...input and technical guidance on product lifecycle planning and regulatory requirements for Class II software medical… more
- Abbott (Plymouth, MN)
- …get on with their lives. **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist ** to join Abbott's Electrophysiology Division on-site ... Paul, MN. 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
- 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
- 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