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About AbbVie
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 www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
We are looking for a QC Lab Supervisor to join our quality team on our AbbVie Cork site for a fixed-term contract of 12 months. In this role you will be leading an experienced team of analysts and senior analysts in the Quality Control department. This will involve planning against operational and supply chain timelines, leading the team in terms of continuous improvement culture and operational excellence mindsets and ensuring that products are released to schedule.
- Oversee laboratory operations, ensuring staff activities are aligned with planning requirements.
- Evaluate analytical results and authorize material release according to established procedures.
- Arrange required validations to meet both national and international standards.
- Direct and supervise maintenance and repair of laboratory equipment.
- Establish and review procedures by developing and revising SOPs, methods, and specifications.
- Perform reviews of documentation, generate reports, and conduct trending to guarantee compliance.
- Contribute to QC department advancement by supporting initiatives, strategic goals, and development plans.
- Ensure QC processes adhere to internal procedures, cGMP, and all applicable safety regulations.
- Stay current on regulatory standards and developments through use of internal resources, regulatory department feedback, training sessions, and relevant websites.
- Compile, report, and communicate QC department metrics and key events to senior management.
- Manage QA-related projects and collaborate on cross-functional initiatives
- Bachelor’s degree in analytical science or a similar science-based field.
- Three to five years of experience working in a quality control laboratory within the pharmaceutical sector, with solid familiarity with current FLI manufacturing processes and practices. Proficiency with ERP computerized systems is required.
- Strong understanding of quality control (QC) regulations and the standards set by regulatory authorities.
- Previous supervisory experience or proven skills in people management.
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.
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