Job Description AbbVie Biologics Ballytivnan seeks a Senior Manufacturing Compliance Specialist to strengthen our Quality Assurance operations.
In this role, you'll help ensure product excellence through quality compliance, incident resolution, and floor-level support within a collaborative manufacturing environment.
Responsibilities Ensure all products and process simulations meet standards for market/investigational use.
Provide quality guidance and compliance oversight throughout manufacturing.
Lead or support investigations related to non-compliance in product or processes.
Mentor, train, and provide support to shift team members.
Audit batch documentation, review logs, and process SOPs.
Support and execute line clearance, raw material checks, and stability program activities.
Manage and maintain finished product status, labeling, and quality logs.
Conduct daily manufacturing area walkarounds and seek process improvements.
Support quality aspects of MVI, AQL, and NPI process/material handovers.
Maintain compliance with cGMP, HPRA/FDA, EHS, and AbbVie standards.
Qualifications Third-level degree in science, quality, or engineering.
Minimum 3 years' experience in a GMP quality/operations setting (biologics preferred).
Strong experience in aseptic processing and advanced knowledge of regulatory requirements.
Excellent written/verbal communication and interpersonal skills.
Experience as a trainer preferred.
Demonstrated commitment to quality, problem-solving, and continuous improvement.
Additional Information 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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