• Regulatory Affairs Specialist

    Abbott (Plymouth, MN)
    …their health and get on with their lives. **The Opportunity** We are recruiting for a ** Regulatory Affairs Specialist III ** to join our team on-site in ... team goals and division regulatory priorities. + Provides support to Regulatory Affairs management when working towards resolution of compliance issues… more
    Abbott (10/17/24)
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  • Regulatory Affairs Specialist

    Abbott (Austin, TX)
    …to work for diversity, working mothers, female executives, and scientists. **The Opportunity** This Regulatory Affairs Specialist III position will work ... and division regulatory priorities. + Provides support to Regulatory Affairs management when working towards resolution of compliance issues assuring these… more
    Abbott (09/19/24)
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  • Regulatory Affairs Specialist

    ThermoFisher Scientific (Cincinnati, OH)
    …Office **Job Description** **How will you make an impact?** The DEA Compliance Specialist III will ensure our Cincinnati site follows the Drug Enforcement ... communication, critical thinking, and problem solving skills. The DEA Compliance Specialist III works closely with manufacturing, development, lab personnel,… more
    ThermoFisher Scientific (10/11/24)
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  • Principal Regulatory Affairs

    Teleflex (Morrisville, NC)
    Principal Regulatory Affairs Specialist **Date:** Oct 3, 2024 **Location:** Morrisville, NC, US **Company:** Teleflex **Expected Travel** : Up to 10% ... solutions that make a difference in patients' lives. **Position Summary** The Principal Regulatory Affairs - Strategic Operations position will focus on the … more
    Teleflex (10/04/24)
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  • Regulatory Affairs Specialist

    Kelly Services (Burnsville, MN)
    Kelly Science and Clinical FSP is currently seeking a Regulatory Affairs Specialist for a long-term engagement with one of our Global Pharmaceutical clients. ... time off, including holiday, vacation, and sick/personal time. This Regulatory Affairs Coordinator will help administer the...the preparation, submissions and approval for Class II and III medical devices in China is preferred. + Strong… more
    Kelly Services (10/01/24)
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  • Sr. Regulatory Affairs

    Teleflex (Chelmsford, MA)
    Sr. Regulatory Affairs Specialist **Date:**...3 years of experience with Class I, II or III medical devices. * Proven history of successful domestic ... that make a difference in patients' lives. **Position Summary** The Sr. Regulatory Affairs Specialist (SRA) will develop US, EU, and Canada strategies,… more
    Teleflex (10/24/24)
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  • Principal Regulatory Affairs

    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
    Abbott (08/18/24)
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  • Senior Regulatory Affairs

    Stryker (Portage, MI)
    …people who deliver safe and robust solutions. **What you will do** As the Regulatory Affairs Specialist , you will support Stryker's Acute Care portfolio ... is available at www.stryker.com . We are currently seeking an **Senior** ** Regulatory Affairs ** **Associate** to join our **Acute Care business unit**… more
    Stryker (08/17/24)
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  • Sr. Specialist , Regulatory

    MicroVention, Inc. (Aliso Viejo, CA)
    …7. Ability to comprehend technical documents and concepts. **External-Facing Title:** Senior Specialist Regulatory Affairs **Posting Country:** US - United ... **12271BR** **Title:** Sr. Specialist , Regulatory Affairs **Job...as evidenced by successful US FDA Class II / III medical device submissions, EU CE Mark applications, Health… more
    MicroVention, Inc. (10/23/24)
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  • Senior Regulatory Affairs

    Stryker (Portage, MI)
    …**Instruments Division** to be based in Kalamazoo, Michigan or remote. As the Senior Regulatory Affairs Specialist , you will provide regulatory support ... projects and deadlines. **Preferred** + Masters in Regulatory Affairs + Knowledge of Class III Devices + PMA + Implantable Devices + Patient Specific Devices… more
    Stryker (10/15/24)
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  • Senior Regulatory Affairs

    Stryker (Redmond, WA)
    …is available at www.stryker.com . We are currently seeking an **Senior** ** Regulatory Affairs Associate** to join our **Medical Division** , **Hybrid** ... **What you will do** As part of the Medical Regulatory Affairs team, you will work with...Affairs role required. + Previous experience with Class II/ III medical devices preferred. + Previous experience drafting 510(k)s… more
    Stryker (08/21/24)
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  • Principal Regulatory Affairs

    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
    Abbott (09/28/24)
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  • Regulatory Specialist III

    MyFlorida (Tallahassee, FL)
    REGULATORY SPECIALIST III - 79010241 Date: Oct 16, 2024 The State Personnel System is an E-Verify employer. For more information click on our E-Verify ... . Requisition No: 839001 Agency: Business and Professional Regulations Working Title: REGULATORY SPECIALIST III - 79010241 Pay Plan: Career… more
    MyFlorida (10/23/24)
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  • Advanced Practice Nurse (Clinical Nurse…

    Veterans Affairs, Veterans Health Administration (Cleveland, OH)
    …must be met to qualify for Advanced Practice Nurse (Clinical Nurse Specialist ) III : Scope: Executes position responsibilities that demonstrate leadership, ... Healthcare System is recruiting for a Advanced Practice Nurse (Clinical Nurse Specialist ). The Advanced Practice Nurse (Clinical Nurse Specialist ) will function… more
    Veterans Affairs, Veterans Health Administration (10/17/24)
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  • Supervisory Biomedical Equipment Support…

    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 (10/23/24)
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  • Pharmacist(Clinical Specialist )

    Veterans Affairs, Veterans Health Administration (Detroit, MI)
    …(EMR) within a progress note. Documentation will be professional and timely. iii . Provides drug information, observations on patient response to therapy, and ... implementation of programs which assure and enhance patient care. iii . Keep abreast of new developments in the field...program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Participation in the Coronavirus… more
    Veterans Affairs, Veterans Health Administration (10/26/24)
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  • Medical Records Technician (Clinical Documentation…

    Veterans Affairs, Veterans Health Administration (Fredericksburg, VA)
    …classes representing their clinical conditions and resource needs. Monitors ever-changing regulatory and policy requirements affecting coded information for the full ... influenza vaccination program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Participation in the Coronavirus Disease 2019… more
    Veterans Affairs, Veterans Health Administration (10/16/24)
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  • Regulatory Specialist (Labeling)…

    LSI Solutions (Victor, NY)
    …II Essential Functions listed above, in an FDA regulated environment (medical devices preferred). Regulatory Specialist III : + Bachelor or Master's degree in ... sciences discipline with 6-7 years' experience, relevant to the Regulatory Specialist III Essential Functions...in an FDA regulated environment (medical devices preferred). + Regulatory Affairs Certification (RAC) a plus, but… more
    LSI Solutions (09/10/24)
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  • Sr. Specialist , Regulatory Project…

    West Pharmaceutical Services (Exton, PA)
    …Requisition ID: 67683 Date: Oct 16, 2024 Location: Exton, Pennsylvania, US Department: Regulatory Affairs Description: **Thank you for your interest in our Sr ... Sr. Specialist , Regulatory Project Management (Evergreen Posting)...Project Management (RPM) role is responsible for management of regulatory affairs projects associated with West's global… more
    West Pharmaceutical Services (10/21/24)
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  • Senior Director, Scientific Medical Affairs

    AbbVie (Mettawa, IL)
    …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Provides specialist medical and scientific strategic and operational input into core medical ... affairs activities such as: healthcare professional/provider interactions (Payers, Patients,...into and influences the development of asset strategy. Provides specialist medical insights, and executes on data generation, communication,… more
    AbbVie (09/21/24)
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