• Merck & Co. (Durham, NC)
    Job DescriptionThe Quality Senior Specialist provides expertise in the coordination of resources and equipment pertaining to qualification/validation activities ... supporting the vaccine expansion facility. Primary Responsibilities: The Quality Senior Specialist will be responsible for comprehensive management of all activities… more
    HireLifeScience (06/18/24)
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  • Merck & Co. (Durham, NC)
    …and requalification activities for multiple pieces of equipment. The Senior Specialist will primarily support vaccine drug manufacturing via Validation program ... Component SuppliersAuthor, review, and/or edit validation documents to support regulatory filingsSupport Change Control documentation for complex process, validation,… more
    HireLifeScience (06/14/24)
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  • Eisai, Inc (Nutley, NJ)
    …mild cognitive impairment due to Alzheimer's disease (AD) or mild AD. TheNeurology Account Specialist (NAS) will be part of a diverse team of sales professionals who ... sales/business analytics, etc.)Strong understanding of pharmaceutical manufacturer compliance & regulatory requirementsDemonstrated success in driving growth and profitability, establishing… more
    HireLifeScience (06/14/24)
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  • Merck & Co. (Rahway, NJ)
    …job that provides both technical and project management responsibility. The Associate Specialist - Engineering Auto Eng position will report to the Director, ... developed through education or experience.Preferred:A working knowledge of the regulatory requirements for pharmaceutical applications.Programming skills in PLCs or… more
    HireLifeScience (06/15/24)
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  • Merck & Co. (Durham, NC)
    …with our incredibly high standards of quality and meets all regulatory requirements.- Partnering across our internal manufacturing facilities, external contract ... and attendant quality control problems. Basic understanding of GMPs and of regulatory requirements as they apply to the vaccine, sterile pharmaceutical or related… more
    HireLifeScience (06/12/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Senior Specialist , Clinical Literature MonitoringProvides pertinent and timely information on our Company's products and ... interests from the world's biomedical literature in support of regulatory , clinical research, marketing, and legal functions.- Plans, organizes, monitors,… more
    HireLifeScience (06/08/24)
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  • Legend Biotech USA, Inc. (Baltimore, MD)
    …the treatment of multiple myeloma. Legend Biotech is seeking a Sr. Cell Therapy Account Specialist - Washington, DC as part of the Commercial team that will be based ... Remotely. Role Overview The Sr. Cell Therapy Account Specialist is responsible for representing Legend's products and services to a defined customer base, generating… more
    HireLifeScience (06/11/24)
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  • Merck & Co. (Rahway, NJ)
    …CCDS, CCPPI, CCIFU) and US labeling for marketed products; and supporting country Regulatory Affairs in the development and maintenance of the EU Labeling and other ... and implementing US Labeling for assigned products in line with regulatory requirements and internal standards and guidelines.- Assisting with developing and… more
    HireLifeScience (06/07/24)
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  • Merck & Co. (Rahway, NJ)
    …Pharmacology and Pharmacometrics --Immune/Oncology-(QP2-IO)-team in the role of-Senior Specialist .--QP2-IO team is part of the Global Clinical Development ... senior scientists you will develop a comprehensive understanding of global regulatory expectations for small molecules and biologics, including support and authoring… more
    HireLifeScience (06/04/24)
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  • Merck & Co. (Durham, NC)
    …Durham employs 1,000+ people. This role as a Training Operations Associate Specialist will be an energetic individual with strong interpersonal, leadership, and ... manufacturing and related systems (ie SAP) Familiarity with pharmaceutical regulatory requirements Project management and data analysis skillsTechnical writing… more
    HireLifeScience (06/06/24)
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  • Merck & Co. (Rahway, NJ)
    …document disclosure, and data sharing with external researchers. - The Specialist (Disclosure Medical Writer) will be primarily responsible for preparing clinical ... documents for clinical studies in all therapeutic areas. - The Specialist will be responsible for: Authoring scientifically valid clinical trial registration… more
    HireLifeScience (06/14/24)
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  • Atrium Health (Charlotte, NC)
    …Staff Overview Job Summary Assists with the coordination of clinical, regulatory , business, and other research- related activities and documentation for clinical ... guidances, GCP and ICH. Essential Functions Assists with clinical, regulatory , business, and other documentation associated with oncology research projects/clinical… more
    JobGet (06/16/24)
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  • The University of Vermont Health Network (Plattsburgh, NY)
    …standards.QUALIFICATIONS: 1.Doctor of Pharmacy degree required.2.Current NYS Pharmacist License required.3.Board of Pharmacotherapy Specialist Certification ... Manager also assists the Director with organizational planning, compliance with regulatory standards, fiscal management setting and maintaining standards of pharmacy… more
    JobGet (05/14/24)
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  • Regulatory Affairs Specialist

    Astrix Technology (St. Joseph, MO)
    Regulatory Affairs Specialist Regulatory Affairs Saint Joseph, MO, US Pay Rate Low: 56.00 | Pay Rate High: 60.00 + Added - 03/06/2024 Apply for Job ** ... Regulatory Affairs Specialist ** Our client is a...materials, product import, pesticide state adverse event reporting, state licensing renewals, state product renewals, and tonnage reporting. +… more
    Astrix Technology (06/05/24)
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  • Accreditation and Regulatory Compliance…

    Lucile Packard Children's Hospital Stanford (Palo Alto, CA)
    …job. In collaboration with the Director of Accreditation, The Accreditation and Regulatory Compliance Specialist manages all aspects of accreditation, ... and project management. Communicates with involved organizational personnel about accreditation/ regulatory requirements, implications to the healthcare environment and strategies… more
    Lucile Packard Children's Hospital Stanford (04/26/24)
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  • Regulatory Specialist II - 1

    MyFlorida (Tallahassee, FL)
    REGULATORY SPECIALIST II - 79011174 1 Date: Jun 10, 2024 Location: TALLAHASSEE, FL, US, 32399 The State Personnel System is an E-Verify employer. For more ... . Requisition No: 830985 Agency: Business and Professional Regulations Working Title: REGULATORY SPECIALIST II - 79011174 1 Pay Plan: Career Service… more
    MyFlorida (06/11/24)
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  • Regulatory Specialist I

    MyFlorida (Tallahassee, FL)
    REGULATORY SPECIALIST I - 79011103 Date: Jun 4, 2024 Location: TALLAHASSEE, FL, US, 32399 The State Personnel System is an E-Verify employer. For more ... . Requisition No: 822339 Agency: Business and Professional Regulations Working Title: REGULATORY SPECIALIST I - 79011103 Pay Plan: Career Service Position… more
    MyFlorida (05/11/24)
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  • Contracts & Regulatory Specialist

    Ardon (Portland, OR)
    As we continue to grow, we are seeking a Contracts & Regulatory Specialist to join our award-winning specialty pharmacy team. About Ardon Health At Ardon, we are ... an elevated role. We are recruiting a Contracts & Regulatory Specialist to join our team of...including but not limited to, portal maintenance, disclosure and license updates, revalidations, and responding to audits and surveys.… more
    Ardon (06/14/24)
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  • RN Policy and Regulatory Specialist

    AccentCare, Inc. (TX)
    Overview Find Your Passion and Purpose as a Policy and Regulatory Specialist -RN Reimagine Your Career in Corporate Healthcare As a professional, you know that ... accounts What You Need to Know The Policy and Regulatory Specialist is responsible for researching and...and common sense. Required Certifications and Licensures: Current RN License Required Come As You Are At AccentCare, our… more
    AccentCare, Inc. (06/09/24)
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  • Clinical Trials Regulatory

    Emory Healthcare/Emory University (Atlanta, GA)
    …community-based research, and laboratory-based translational human immunology. The Clinical Trials Regulatory Specialist I is an entry-level position supporting ... non-interventional studies, with a relatively small trial portfolio. KEY RESPONSIBILITIES: + Assists regulatory team ( Regulatory Specialist II and III) in… more
    Emory Healthcare/Emory University (05/31/24)
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