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Quality manager, programme management

Cork
AbbVie
Programme manager
Posted: 17h ago
Offer description

Quality Manager, Programme Management
Join to apply for the Quality Manager, Programme Management role at Abb Vie
Company Description
Abb Vie'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 Abb Vie, please visit us at www.abbvie.com.
Follow@abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok.
Job Location
Cork, County Cork, Ireland
Job Description
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 organization 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.
Lead 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.
Lead Opex initiatives across the Quality Department.
Qualifications
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.
Abb Vie 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 applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html
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