• Merck & Co. (Rahway, NJ)
    …reported are in compliance with the GLPs and GCPs or other applicable regulatory requirements, as well as study protocols, SOPs, and industry guidance and ... related experience, with at least 1 year of auditing experience in the regulatory compliance environment.SCOPE MEASURES: This position is key to the completion of… more
    HireLifeScience (01/07/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Maintenance Specialist I (2nd or 3rd shift) as part of the Facilities & Engineering ... thermal energy principals, mechanical maintenance techniques, and electromechanical theoryEnsures regulatory and job training remains current by promptly completing… more
    HireLifeScience (12/11/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma.Legend Biotech is seeking QC Microbiology Technical Specialist I/II/III as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QC Microbiology Technical Specialist is an exempt level position with responsibilities for tracking and managing all CAPA's, corrections and change… more
    HireLifeScience (11/13/24)
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  • Merck & Co. (Rahway, NJ)
    …integrating strategic and tactical input from diverse disciplines (eg, clinical, regulatory , market access, manufacturing, CMC, commercial, and other areas) as ... the information that they need. - Providing mentoring, coaching, and oversight to Specialist and Senior Specialist project managers working on common projects.… more
    HireLifeScience (01/03/25)
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  • Regulatory Specialist

    Kelly Services (Bridgewater, NJ)
    …**egulatory Affairs Specialist ** Kelly(R) Science & Clinical is seeking a Regulatory Affairs Specialist for our client a leading medical device Bridgewater, ... role - 3 days in the office** **Overview** Responsible for providing Regulatory Affairs support to International RA Teams for product registrations, renewals to… more
    Kelly Services (12/17/24)
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  • Senior Regulatory Affairs Specialist

    Stryker (Mahwah, NJ)
    …We are currently seeking a **Senior Regulatory Affairs Specialist ** to join ... and interact with regulatory agencies and notified bodies. The Senior Regulatory Affairs Specialist is the Regulatory SME on cross-functional teams and a… more
    Stryker (12/17/24)
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  • Senior Regulatory & Compliance…

    Catalent Pharma Solutions (Somerset, NJ)
    **Position Summary:** Catalent Pharma Solutions in Somerset, NJ is hiring a Senior Regulatory and Compliance Specialist for the Regulatory Affairs Group. The ... Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry and their impact on… more
    Catalent Pharma Solutions (12/27/24)
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  • Specialist , Regulatory Science…

    Robert Half Technology (Mahwah, NJ)
    Description We are offering a long-term contract employment opportunity for a Regulatory Science Specialist . This role is based in Mahwah, New Jersey and is ... and external suppliers, as well as compliance with cGMP/cGDP, safety, and regulatory requirements. Key responsibilities: * Author and execute protocols, while also… more
    Robert Half Technology (12/30/24)
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  • Distribution Regulatory Specialist

    ThermoFisher Scientific (Bridgewater, NJ)
    …**Job Description** **A day in the Life:** + Supervise and lead regulatory compliance for hazardous materials distribution, including DOT, IATA, IMDG, and other ... + Conduct regular audits and inspections to ensure full regulatory compliance and identify areas for improvement. + Train...for improvement. + Train and guide team members on regulatory updates and standard methodologies. + Serve as the… more
    ThermoFisher Scientific (12/30/24)
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  • Regulatory Specialist

    Actalent (Mahwah, NJ)
    …New Jersey seeking a 6-12 month contractor to help support their Regulatory department! Position Overview: + Support manufacturing of orthopedic medical device ... suppliers. + Conducts work in compliance with cGMP/cGDP, safety and regulatory requirements. Qualifications: + Knowledge of medical devices, concepts of… more
    Actalent (01/03/25)
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  • Specialist , Regulatory Science…

    Actalent (Mahwah, NJ)
    …and/or external suppliers. -Conducts work in compliance with cGMP/cGDP, safety and regulatory requirements. Skills regulatory , regulatory submission, gmp, ... regulatory compliance, batching Top Skills Details regulatory , regulatory submission,gmp Experience Level Expert Level Pay and Benefits The pay range for this… more
    Actalent (01/03/25)
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  • Clinical Research Coordinator

    Hackensack Meridian Health (Edison, NJ)
    …+ Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... compliant study conduct according to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures. This role carries… more
    Hackensack Meridian Health (12/06/24)
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  • Consumer Lender - Support

    Robert Half Accountemps (Edison, NJ)
    Description Robert Half is currently seeking a regulatory compliance specialist for a job opportunity located in the Woodbridge, NJ area. As a Compliance ... Specialist , you will be responsible for ensuring our company...including MS Power Point and MS Excel. * Certified Regulatory Compliance Manager (CRCM) certification is highly preferred. Requirements… more
    Robert Half Accountemps (12/06/24)
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  • Senior Manager, Medical Writing, Oncology

    Gilead Sciences, Inc. (Parsippany, NJ)
    …projects. You will represent Medical Writing on relevant product, project, and/or regulatory submissions teams; providing specialist guidance on the optimal ... + Recognized as a SME in a broad range of regulatory documentation and a resource for specialist advice and guidance. + In-depth knowledge of relevant health… more
    Gilead Sciences, Inc. (11/18/24)
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  • Associate Director, Medical Writing

    Gilead Sciences, Inc. (Parsippany, NJ)
    …projects. You will represent Medical Writing on relevant product, project, and/or regulatory submissions teams; providing specialist guidance on the optimal ... a subject matter expert in a broad range of regulatory documentation and a resource for specialist ...of regulatory documentation and a resource for specialist advice and guidance. + Demonstrates in-depth knowledge of… more
    Gilead Sciences, Inc. (11/15/24)
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  • Peer Recovery Specialist , START Program

    The Center for Great Expectations (Bridgewater, NJ)
    Peer Recovery Specialist , START Program Bridgewater, NJ (http://maps.google.com/maps?q=120+Finderne+Avenue+Bridgewater+NJ+USA+08807) Job Type Full-time Description ... Peer Recovery Specialist , START Program Support for mothers with substance use...+ Maintain records as required by organization policies and regulatory and accrediting agencies. + Assist individuals in areas… more
    The Center for Great Expectations (01/04/25)
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  • Raw Material and Supplier Quality Management…

    Vantage Specialty Chemicals (Warren, NJ)
    …**Job Overview:** The Raw Materials and Supplier Quality Management Senior Specialist will develop and implement the company's supplier policy focusing on ... regulatory , quality, and document requirements. This position will work...Implementation:** + Develop and maintain supplier policies covering quality, regulatory , and documentation requirements. + Ensure alignment of supplier… more
    Vantage Specialty Chemicals (10/30/24)
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  • Senior Supervisory Control Specialist

    Wells Fargo (Bedminster, NJ)
    **About this role:** Wells Fargo is seeking a Senior Supervisory Control Specialist to join our Client Relationship Group within Wealth and Investment Management. ... will ensure the firms' requirements for supervision are in adherence with regulatory , compliance and legal requirements. The Senior Supervisory Control Specialist more
    Wells Fargo (12/18/24)
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  • Pharmacovigilance (PV) Analytics and Reporting…

    US Tech Solutions (Madison, NJ)
    **Title:** **Pharmacovigilance (PV) Analytics and Reporting Specialist ** **Duration : 12 Months contract** **Role:** **Must be onsite 50% at Lawrenceville, NJ ... is Onsite (Lawrenceville/New Brunswick)** Pharmacovigilance (PV) Analytics and Reporting Specialist , PV Analytics Center of Excellence - JD The Pharmacovigilance… more
    US Tech Solutions (10/18/24)
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  • Quality Specialist

    ManpowerGroup (Bridgewater, NJ)
    Our client, a leader in the healthcare industry, is seeking a Quality Specialist to join their team. As a Quality Specialist , you will be part of the Quality ... to work collaboratively with cross-functional teams. **Job Title:** Quality Specialist **Location:** Bridgewater, NJ **Pay Range:** Competitive **What's the Job?**… more
    ManpowerGroup (01/07/25)
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