- DivIHN Integration Inc (Green Oaks, IL)
- …please contact one of our Talent Specialists Meghna at ### Rashi at ### Title: Regulatory Affairs Specialist Location: Abbott Park, IL Duration: 7 Months ... protocols/reports. Review and approval of manufacturing changes for Class III implantable medical devices. May require an advanced degree...role As an individual contributor, the function of a Regulatory Affairs Specialist is to… more
- DivIHN Integration Inc (North Chicago, IL)
- …please contact one of our Talent Specialists Meghna at ### Rashi at ### Title: Specialist Regulatory Affairs Duration: 7 Months Location: Abbott Park, IL/ ... head of a unit/department. Accountability / Scope: As the professional in the Regulatory Affairs function, the individual will assist teams in the registration… more
- ThermoFisher Scientific (Asheville, NC)
- …they need to take science a step beyond. **Discover Impactful Work:** The Regulatory Specialist is accountable for global product compliance through design ... Bachelor's degree or 4+ years of experience in product compliance, quality, regulatory affairs , or engineering. **Suggested Experience** + Involvement with… more
- Medtronic (Santa Rosa, CA)
- Principal Regulatory Affairs Specialist - Structural Heart and Aortic, Mitral and Tricuspid (hybrid) Come be a part of one of the most exciting therapy areas ... Affairs team and looking to hire a Principal Regulatory Affairs Specialist to make...life cycle. + Medical device industry experience with Class II/ III /IV products. + Experience supporting software device development (for… more
- Medtronic (Minneapolis, MN)
- Position Description: Sr. Regulatory Affairs Specialist for Medtronic, Inc. Minneapolis, MN. Multiple positions available. Responsible for developing ... PMA (Pre-Market Approval) or 510(k) submissions for US Class III or Class II medical devices. Work on MDD...closely related field and 2 years' experience as a Regulatory Affairs Specialist , R&D Engineer… more
- Medtronic (Northridge, CA)
- …90,000+ employees in more than 160 countries. **A Day in the Life** As Principal Regulatory Affairs Specialist , you will develop and implement medical device ... agencies. + As an individual contributor, the Principal Regulatory Affairs Specialist is responsible...strategies for new and modified Class IIa & Class III devices and preparing and submitting regulatory … more
- ConvaTec (Lexington, MA)
- …Convatec, please visit http://www.convatecgroup.com **Job Summary:** In this role as a Senior Regulatory Affairs Specialist at Convatec, you will be ... Technologies division's global regulatory strategies and processes. The Senior Regulatory Affairs Specialist will drive compliance, mentor colleagues,… more
- Abbott (Atlanta, GA)
- …mothers, female executives, and scientists **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist ** to join Abbott's Heart Failure ... Division. As an individual contributor, the Principal Regulatory Affairs Specialist is responsible... regulatory guidance to cross-functional partners, developing global regulatory strategies for new and modified Class III… more
- Abbott (Pleasanton, CA)
- …mothers, female executives, and scientists **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist ** to join Abbott's Heart Failure ... Pleasanton, CA. As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to...5 years' experience working with Class II and/or Class III medical devices. Regulatory Affairs … more
- Amazon (Bellevue, WA)
- …Frames. Working as part of the Medical Devices Operational Compliance Team (MD-OCC), the Sr. Regulatory Affairs Specialist will be working to build best in ... industry with experience working with Class II and/or Class III devices. - . Ability to work effectively on...dollar businesses and reporting to senior leadership - . Regulatory Affairs Certification (RAPS) - . Drug… more
- Cordis (Irvine, CA)
- …strong working relationships with internal and external customers. **Responsibilities** * The Regulatory Affairs Specialist (RAS) is responsible for the ... equivalent professional experience. * 2+ years of experience in regulatory affairs in medical device/pharmaceutical industry, GLP,...* Experience in FDA / EU regulations for class III medical device * Analytical and Critical Thinker *… more
- Bausch + Lomb (O'Fallon, MO)
- …advancement of eye health in the future. **Objectives:** Responsible for providing Regulatory Affairs support under direct supervision supporting regulatory ... such as biology, chemistry, physiology, engineering, medical or law or related regulatory affairs experience with medical devices or pharmaceuticals + Minimum… more
- MyFlorida (Miami, FL)
- REGULATORY SPECIALIST III - 79000823 Date: Apr 27, 2024 Location: MIAMI, FL, US, 33055 MIAMI, FL, US, 33135 MIAMI, FL, US, 33155 MIAMI, FL, US, 33132 MIAMI, ... . Requisition No: 825227 Agency: Business and Professional Regulations Working Title: REGULATORY SPECIALIST III - 79000823 Pay Plan: Career… more
- Veterans Affairs, Veterans Health Administration (Orlando, FL)
- Summary The Supervisory Biomedical Equipment Support Specialist (BESS) works in support of the Healthcare Technology Management (HTM) Service by providing ... The major duties and responsibilities of a Supervisory Biomedical Equipment Support Specialist include, but are not limited to: Lifecycle management of any and… more
- Veterans Affairs, Veterans Health Administration (Nashville, TN)
- …requirements. Click here for more information about the Department of Veterans Affairs 's Recent Graduate Program. Responsibilities The position serves as a Health ... System Specialist (GHATP Trainee) within a one year formalized national...events either separately or in conjunction with the Public Affairs Office. Displays knowledge of VA priorities and mission… more
- ThermoFisher Scientific (Middletown, VA)
- …Group (SDG) **How will you make an impact?** The Medical Device Complaint Handling Specialist III is responsible for managing and resolving complaints related to ... requirements + Collaborate with cross-functional teams, including Quality Assurance, Regulatory Affairs , and Product Development, to resolve complaints. +… more
- BioFire Diagnostics, LLC. (Salt Lake City, UT)
- …and reviews escalated complaints for potential reportable events. + Coordinates with regulatory affairs to complete reportable event documentation. + Review ... trend charts and perform data analysis. + Work with experts from other departments during investigation process. + Review complaints for CAPA. + Conduct product literature review and work with other departments to address product performance in the field. +… more
- State of Colorado (Denver, CO)
- Contract Administrator III - Multiple Positions Print (https://www.governmentjobs.com/careers/colorado/jobs/newprint/4463188) Apply Contract Administrator III ... Job Type Full Time Job Number NAA-CAIIIEXT-04.2024 Department Department of Local Affairs Opening Date 04/09/2024 Closing Date 6/24/2024 11:59 PM Mountain FLSA… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …Clinical Trials Regulatory Specialist I is an entry-level position supporting regulatory affairs in clinical trial research. + The primary focus of the ... small trial portfolio. + Duties include: + Assists regulatory team ( Regulatory Specialist II and III ) in research efforts by facilitating the protocol… more
- Methodist Health System (Dallas, TX)
- …**Days Of Week :** M-F **Work Shift :** **Job Description :** Your Job: The Regulatory Specialist will perform expertise in the regulatory component of all ... trials (IITs), and retrospective analysis of clinical data. The Regulatory Specialist will support the mission, vision,...research (required) * 1 year of experience in research regulatory affairs (required) * Strong proficiency using… more
Related Job Searches:
Affairs,
Affairs Specialist,
Regulatory,
Regulatory Affairs,
Regulatory Affairs Specialist,
Specialist,
Specialist III