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 including immunology, oncology and neuroscience
- and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. Issue production batch records, worksheets, packaging records, and related controlled documents using approved systems and current effective versions. Ensure only current, approved documentation is issued for manufacturing use. Print, prepare, stamp, and control manufacturing documentation according to site procedures. Maintain document accountability, issuance logs, and controlled records. Support Manufacturing, Planning, Quality Assurance, and Process Sciences by preparing records for scheduled production activities. Process requests for additional pages,



replacement documentation, and document revisions while maintaining traceability. Verify issued documentation is complete, legible, accurate, and attributable to the correct batch. Maintain compliance with GMP, GDP, Data Integrity, and document control requirements. Support investigations, audits, inspections, and document retrieval requests as required. (The procedures establish controlled-document accountability and retention activities.) SAP Electronic Document Management Systems (eDMS/Vault) Experience with document control and records management. Ability to work with Manufacturing, QA, Planning, and Supply Chain teams. Proficiency with SAP and document management systems. Robust organizational and compliance mindset. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.

📌 Documentation and Compliance Specialist (Westport)
🏢 AbbVie
📍 Westport