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AbbVie

QA Specialist

AbbVie Cork, Munster, Ireland

Pharmaceutical Manufacturing · 10,001+ employees

5 h ago
qa Mid (2-5 yrs) Full-time Contractor Ireland
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About the role

The QA Specialist will provide quality assurance support for pharmaceutical products, medical devices, and biologics, ensuring compliance with corporate and governmental regulations. Responsibilities include managing quality systems, investigating deviations, coordinating audits, and overseeing supplier qualification programs.

What they look for

Quality Assurance Regulatory Compliance GxP Risk Management CAPA Supplier Qualification Product Complaints Data Analysis Quality Systems Auditing Cold Chain Management SolTraqs EBR SAP Technical Writing Cross-functional Collaboration

Requirements

Candidates should possess a Bachelor’s degree in a scientific or engineering field and at least 3 years of experience in quality assurance. Proficiency in GxP compliance, enterprise systems like SAP, and strong communication skills are essential for this role.

Full description

Company Description

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.

Job Description

We are looking for a QA Specialist to join our Quality Assurance team in Cork on a Fixed Term Contract until September 2027.

As a QA Specialist you will be responsible for providing quality assurance support for quality system requirements associated with: pharmaceutical products, medical devices, combination products and biologics. Specific areas of support may include Storage and Distribution, Product Complaints, potential quality events/product shortage execution, Supplier Controls, Product Quality Review, Risk Management, Agency inspections/internal audits, CAPA, and overall Quality Manual requirements. This position will ensure that all product, process or system related quality activities supporting the business at the affiliate from receipt of final product through distribution are in compliance with Corporate, governmental, and local regulations and requirements.

Responsibilities:

  • Assist with the integration and support of quality regulations: drug, biologics, device and/or combination products.
  • Assist in the design of effective quality systems, procedures and/or processes within cross functional teams to ensure compliance as well as efficiency throughout our quality systems. Evaluate, analyze and trend quality indicators, data and performance metrics; communication and elevation of affiliate compliance status and risk while maintaining a continuous improvement objective.
  • Partner, coordinate and support activities related to product actions in the affiliate.
  • Assist project teams in planning, preparation, review and approval of quality documentation. Coordinate the Management Review process for the affiliate.
  • Perform assessments to determine compliance to processes, procedures and regulations to identify potential gaps and mitigate and implement improvements. Support internal and external quality inspections and audits including reporting, response to observations and tracking of action plans.
  • Participate in training and education programs for various aspects of quality assurance.
  • Coordinate and investigate quality events such as deviations, non conformance, product complaints and corresponding action plans including decisions.
  • Quality management of supplier qualification program including performance monitoring for key suppliers.
  • Ensure metrics and KPIs are being met. Provide guidance and support for all activities governed by Good Storage and Distribution Practices including monitoring of controlled temperature and cold chain shipments.
  • Represent affiliate QA in regional, global and cross functional teams, projects and programs, as assigned by management.

Qualifications

  • Bachelor’s Degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering or other technical/scientific area preferred.
  • 3+ years’ experience in quality assurance, quality oversight or relevant experience.
  • Technical knowledge in as many of the following areas as possible: Quality, Regulatory, Process Sciences, Manufacturing Operations.
  • Knowledge and familiarity with product, process, and both internal and external customer requirements.
  • Knowledge of QA systems and GxP compliance requirements including regulations and standards affecting device, biologics and pharmaceutical products preferred.
  • Strong oral and written communication skills needed.
  • Strong computer skills and knowledge of enterprise systems such as SolTraqs, EBR & SAP.

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

  • Workday Global Grade: 13

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