What AbbVie Has to Offer: Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.
Job Details
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.
We are currently seeking an experienced Quality Manager, Programme Manager to join our team in Cork, leading and enhancing the quality culture at our site. As a Quality Manager, you'll drive key quality programs, ensure compliance with industry standards, and help our organisation achieve its quality goals while supporting business objectives.
Responsibilities:
- Lead, coordinate, and manage Key Quality Projects and Programs across the site.
- Oversee quality planning, risk assessments, and approval of key documentation (SOPs, protocols, CAPAs, etc.).
- Ensure compliance and inspection readiness for regulatory agencies (HPRA/FDA) and internal standards.
- Analyse quality data and metrics to support continuous improvement.
- Leading strategic global and capital investments (Quality Lead)
- Support health, safety, and environmental programs by adhering to company and regulatory guidelines.
- Provide technical leadership and guidance to quality and cross-functional teams.
- Leading Opex initiatives across the Quality Department.
- Degree or higher in a Quality or Science-related discipline.
- At least 8 years of experience in quality or manufacturing, with significant leadership experience (4+ years in project or people management).
- Strong knowledge of GMP, compliance, and quality risk management principles.
- Experience with sterile/OSD manufacturing and large product transfers preferred.
- Excellent attention to detail, problem-solving, and communication skills.
- Demonstrated ability to work independently, prioritise tasks, and drive results.
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.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Together, we break through We believe the paths we take to achieving our breakthroughs matter. At AbbVie, every one of our 50,000 employees is a... Read more