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Regulatory Compliance Specialist

Cynet Systems

Regulatory Compliance Specialist

Titusville, NJ
Full Time
Paid
  • Responsibilities

    Job Description

    We are looking for REGULATORY COMPLIANCE SPECIALIST - REMOTE / TELECOMMUTE for our client in TITUSVILLE, NJ

    JOB TITLE: REGULATORY COMPLIANCE SPECIALIST - REMOTE / TELECOMMUTE

    JOB LOCATION: TITUSVILLE, NJ

    JOB TYPE: CONTRACT

    JOB DESCRIPTION:

    • An opportunity has arisen for a Contractor Global Labeling Product Leader (GLPL) to support the products in Company R&D within the Global Labeling Centre of Excellence (GL CoE).

    RESPONSIBILITIES:

    • Responsibilities include development of target labeling, managing the development of updates to Company Core Data Sheets (CCDSs), Centralized/MRP EUPIs, and USPIS in accordance with GL CoE and GRA end-to-end labeling processes.
    • System and business process training will be provided to the Contractor.
    • Facilitation of Labeling Negotiations with Health Authorities for EUPI and USPI for the Assigned product(s); facilitating LWG review and LC endorsement of labeling documents; preparation and finalization of submission-ready EUPI and USPI.
    • Processing Local Labeling Deviation requests for assigned products for ex-US and ex-EU markets, including facilitating LWG review and LC.
    • Preparing updates to the CCDS, EUPI, and USPI for products in additional therapeutic areas (for new indications, safety updates, CMC revisions), including facilitating LWG review and LC endorsement of the CCDS and finalizing/releasing the CCDS.

    QUALIFICATIONS, EXPERIENCE, AND SKILLS:

    • Minimum of Bachelor’s degree in a scientific discipline. Advanced degree (MS, PharmD, Ph.D., or MD) desirable.
    • At least 6 years experience in the pharmaceutical industry or health authority, with at least 5 years experience in regulatory affairs with direct experience associated with product labeling (prescribing and patient information) is preferred.
    • Product labeling experience should include authoring text for inclusion in CCDSs, in addition to APIs, and/or USPIS, including drafting text based on scientific source data, supporting rationale, regulatory requirements, standards, and templates, and liaison with subject matter experts and regulatory professionals.
    • Advanced Microsoft Word skills.
    • Experience working in a Documentum-based document management system.
    • Basic Excel and PowerPoint skills.
    • Excellent project management, verbal, and written communication skills.

    Company Description

    visit our career site to see all open positions @ http://jobs.cynetsystems.com