Join to apply for the Incoming Quality Assurance Supervisor role at AbbVie
Company Description
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.
Job Description
AbbVie Biologics Ballytivnan in Sligo invites applications for the Incoming Quality Assurance Supervisor role in our Quality Assurance department. Reporting to the Quality Operations Manager, this position is pivotal in ensuring materials released for both marketed and investigational drug products meet stringent AbbVie standards. You will oversee the IQA process, lead investigations, support continuous improvement, and collaborate across teams to drive quality, safety, and compliance.
Responsibilities
Oversee and ensure timely, compliant release of all incoming materials for manufacturing
Manage and provide guidance on sampling requirements, especially for aseptic processes
Lead IQA‑related investigations and coordinate with contract laboratories
Review, audit, and author material release records, specifications, and SOPs
Act as site SME for SAP inspection plans and material management; support internal and regulatory audits
Drive process simplification and improvements
Guide cross‑functional and cost improvement initiatives, championing quality in new product introductions
Supervise up to five team members, fostering collaboration and maintaining a high standard of work
Promote and uphold EHS policies, supporting a culture of safety excellence
Qualifications
Bachelor’s degree or above in science, quality, or engineering
At least 3 years of experience in GMP‑regulated quality or operations roles in pharma or biopharma industries
Desired: Previous people supervision
Strong regulatory knowledge, attention to detail, and effective problem‑solving skills
Proven cross‑functional collaboration, leadership ability, and solid communication skills
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. 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
Seniority level
Mid‑Senior level
Employment type
Full‑time
Job function
Quality Assurance
Pharmaceutical Manufacturing and Biotechnology Research
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