- AbbVie (Irvine, CA)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Regulatory Affairs - Device /Combination products supports regulatory ... Provide support to submission activities for a variety of device regulatory approvals including CE mark, US...with eCTD tools and EDMS applications. + Background in regulatory affairs , manufacturing, marketing, or quality assurance… more
- BD (Becton, Dickinson and Company) (Covington, GA)
- **Job Description Summary** As Associate Director, Regulatory Affairs , you will be responsible for managing a team that develops and executes the strategy ... Quality and Regulatory Affairs . International Regulatory Affairs and Senior Leadership....Affairs , and/or a combination of Regulatory Affairs and Quality Assurance within the Medical Device… more
- Sanofi Group (Cambridge, MA)
- About the Role The Associate Director, US Regulatory Affairs ( RA ) serves as the regulatory lead on relative Review Committees (RCs), for products in ... prescription drugs and biologics. Essential Functions + Represents Global Regulatory Affairs (US RA AdPromo)...device industry; this must include extensive experience providing regulatory input and evaluation as part of a promotional… more
- AbbVie (Lake Bluff, IL)
- …stay current with Global industry trends and best practices in combination product and device regulatory affairs , review and comment on changing regulation ... Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director, Regulatory Affairs , Strategic Global Labeling -… more
- ManpowerGroup (Lake Bluff, IL)
- …at Experis IT Manpower Group. Our client, Medical device manufacturing is seeking a Regulatory affairs associate to join their team. Reg Affairs , IVD ... Management, and previous Abbott would be ideal **Job Title: Regulatory Affairs Associate ** **Pay Range:...related to submissions and approvals. + Offers country specific regulatory support **Stakeholders:** + Direct interaction with RA… more
- Abbott (St. Paul, MN)
- …catheters and software, vessel closure devices and peripheral stents. **The Opportunity** This ** Associate Director Regulatory Affairs ** will work on-site at ... Vascular Division. As a manager, the function of an Associate Director Regulatory Affairs is...internal stakeholders. + Consults with and provides advice to senior management of the Company on strategies and plans… more
- AbbVie (Irvine, CA)
- …on Clinical Outcome Assessment (COA) tools including digital and submission activities for device regulatory approvals in a variety of counties including EU, US, ... the key regulatory contact for Quality, Medical Safety and International Regulatory Affairs colleagues. + Provides regulatory policy, intelligence… more
- Lilly (Indianapolis, IN)
- …areas relevant to drug discovery or development, eg epidemiology, toxicology, pharmacovigilance, regulatory affairs + Experience within Global Patient Safety or ... communities through philanthropy and volunteerism. **Purpose:** The purpose of the Medical Device Safety Scientist Associate Director role is to leverage… more
- Takeda Pharmaceuticals (Lexington, MA)
- …JD) preferred. * You have a minimum of 4 years' experience in drug, biologic or device Regulatory Affairs or related field, including a minimum of 2 years' ... potential issues. **Position Accountabilities:** * Collaborate with colleagues in Regulatory Affairs , Medical, Legal, Commercial, and Compliance organizations… more
- Abbott (Alameda, CA)
- …shipment of study devices and supplies to clinical sites and performing study device accountability. + Responsible for assisting senior staff in planning study ... for diversity, working mothers, female executives, and scientists. **The Opportunity** The Senior CRA will assist in the clinical execution and management of all… more
- Abbott (Alameda, CA)
- …staff, and clinical management. + Working knowledge of CFR, ICH-GCP, Clinical and Regulatory Affairs + Flexibility in daily activities. + Proficient with ... devices and supplies to clinical sites. + Perform study device accountability and reconciliation. + Assist senior ...and final reviews of study data in preparation of regulatory submissions. + May interact with RA /QA… more
- Integra LifeSciences (Princeton, NJ)
- …and evaluations + Monitors product development progress with engineering, manufacturing, regulatory affairs and related departments to ensure product line ... help improve outcomes. **SUPERVISION RECEIVED** Under direct supervision of Associate Director, Global Marketing - Surgical Reconstruction, TT **SUPERVISION… more
- Abbott (Alameda, CA)
- …team members, peers, and management. + Working knowledge of GCP, Clinical and Regulatory Affairs . + Flexibility in daily activities. + Proficient with Microsoft ... **The Opportunity** We are looking for a Clinical Research Associate I, to support the Study Start Up team....device group as required. + Responsible for assisting senior study startup staff during site selection. + Maintain… more
- Abbott (Alameda, CA)
- …shipment of study devices and supplies to clinical sites and performing study device accountability. + Responsible for assisting senior staff in planning study ... their glucose levels with our new sensing technology. **The Opportunity** The Associate Clinical Research III will assist in the clinical execution and management… more