<p>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.</p> <p>Job Description</p> <p>We are currently looking for QA & Document Controller Administrator to join our manufacturing site in Carrigtwohill Cork. The candidate will provide a Document Control Service for the Cork Site and an Administration</p> <p>Service to the QA Department, ensuring compliance with cGMP requirements and internal procedures.</p> <p>Role & Responsibilities:</p> <ul> <li>Manage Document Control for the Cork Site through the system </li></ul> <p>including support, training, and development.</p> <ul> <li>Ensure issue, control, withdrawal, distribution, and destruction of </li></ul> <p>controlled document copies across departments.</p> <ul> <li>Co-ordinate the periodic document reviews and file Master Copies. </li><li>Serve as the first point of contact during audits regarding Document Control </li></ul> <p>queries.</p> <ul> <li>Administer Documentum for QA Department. </li><li>Issue and bind batch records for Production, manage archival both onsite and </li></ul> <p>offsite</p> <ul> <li>Maintain QA Department files, archive systems, and office supply levels. </li><li>Prepare QA documents such as SOPs and Quality Agreements. </li><li>Print and maintain labels, prepare reports, documents, and presentations as </li></ul> <p>needed.</p> <ul> <li>Compile KPIs and information for Annual Product Reviews. </li><li>Site Representative for Documentation COE </li><li>Assist QA Department preparations for Regulatory and Corporate Audits. </li><li>Participate in development and continuous improvement initiatives for QA and </li></ul> <p>GMP compliance.</p> <ul> <li>Support to Site training Specialist as required </li><li>Adapt duties as needed based on changes in the group and its business. </li></ul> <p>Qualifications</p> <ul> <li>Proficiency in PC skills and intermediate level use of MS Office suite (Word,Excel, Outlook & PowerPoint). </li><li>Experience using an EDMS computerised solution is essential </li><li>Excellent verbal and written communication skills. </li><li>Leaving Certificate minimum , Science related degree preferred </li></ul> <p>Additional Information</p> <p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.? Equal Opportunity Employer/Veterans/Disabled.</p> <p>US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p> <p>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p> <p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p> <p>Salary:</p>