Compliance Specialist

Job description

Responsible for assisting with the internal audit system that will assure that all production and support functions at the manufacturing facility operate in compliance with all applicable regulations and standards. Responsibilities • Assists with planning and conducting internal compliance audits of all operations within the facility. • Provides support with company and regulatory agency (i.e. DEA, FDA) inspections. • Follow up on audits to assure that action plans are developed and completed in a timely fashion. • Assist with management review and associated metrics for the plant • Provides support in the metrics collection and analysis for compliance-related corrective and preventive actions (CAPA’s). • Responsible for supplier qualifications including new suppliers, changes and re-qualifications. • Bachelor’s Degree, preferably in Science or Engineering, or equivalent related work experience is required. • 3+ years of Biopharmaceutical experience • Quality Assurance/Regulatory Affairs/Compliance is preferred • Knowledge of regulations and standards for pharmaceuticals (e.g. CFR, MCA, DEA). • Must have some knowledge of plant and company level procedures. • Ability to evaluate quality, production and support areas for compliance to GMPs. BOPs, etc. • Ability to identify and investigate problems and help to resolve them. AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok .