- Abbott (Atlanta, GA)
- …a best place to work for diversity, working mothers, female executives, and scientists This ** Regulatory Affairs Specialist II ** will work on-site out of ... + 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
- Seattle Children's (Seattle, WA)
- Serves as a subject-matter expert in quality assurance and regulatory support for clinical research at Seattle Children's Research Institute. Guides and supports all ... submission to local and commercial IRBs. Assesses, analyzes, and implements regulatory requirements, policies, and guidance documents; creates and follows standard… more
- Cook Medical (Winston Salem, NC)
- Overview The Regulatory Affairs Specialist II develops regulatory strategies,obtains and maintains approvals, and serves as a communication liaison ... situations and environments with minimal supervision. Qualifications * Minimum 2 years regulatory affairs experience with medical devices* Bachelor's degree in… 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
- 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
- Actalent (Davis, CA)
- Job Title: Regulatory Affairs Specialist Looking...a candidate that has at least 2-5 years of regulatory experience within Medical Device Class II . ... registrations, ISO 13485 knowledge Location:Davis, CA Responsibilities: + Oversee the regulatory affairs process for new and existing diagnostic products,… more
- Abbott (Plymouth, MN)
- …on with their lives. **The Opportunity** Abbott is seeking a passionate, experienced **Senior Regulatory Affairs Specialist ** to join our team on-site in ... Plymouth, MN. In this role, you will lead the preparation and submission for regulatory approvals and identify and resolve problems. You will provide regulatory … more