69 Qualified jobs in Ireland
Qualified / Part Qualified Accountant
Posted 11 days ago
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Part Qualified/Qualified Accountant
Posted 11 days ago
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Part Qualified/Newly Qualified Accountant
Posted 5 days ago
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Part Qualified or Qualified Accountant
Posted 6 days ago
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Qualified Person

Posted 14 days ago
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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 Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
The Qualified Person (QP) at AbbVie Biologics Ballytivnan Sligo is responsible for ensuring the compliance and quality of our pharmaceutical products. This role requires expertise in quality assurance practices within an FDA and EMEA approved environment to maintain product safety and integrity. As a QP for the site, you will work closely with our products throughout their manufacturing lifecycle, up until release from the site.
Responsibilities
+ Ensure compliance with EudraLex Volume 4 EU Guidelines for Good Manufacturing Practice and Annex 16 requirements.
+ Certify that each batch is manufactured and checked according to relevant laws, GMPs, and product specifications at AbbVie Biologics Ballytivnan Sligo.
+ Oversee the disposition of bulk products, determining release or rejection based on manufacturing and testing data.
+ Assess and resolve day-to-day quality issues, ensuring products meet quality and safety standards.
+ Support cross-functional teams in process improvement and cost efficiency initiatives.
+ Provide technical leadership and collaborate with stakeholders to enhance product quality and process optimization.
+ Make informed decisions within quality systems, adhering to regulatory standards, and handle quality queries from the operations team.
+ Promote a culture of excellence in quality and compliance throughout the organization.
+ Participate in internal and external audits, ensuring readiness and compliance with quality standards.
Qualifications
+ Essential: Bachelor's degree in a science discipline and a minimum of 5 years of experience in the pharmaceutical industry.
+ MSc in Industrial Pharmaceutical Science or equivalent recognized for QP status under Directive 2001/83/EC, Article 49.
+ Experience as a QP on a license preferrable
+ Experience in aseptic processing and quality functions.
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 & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
Qualified Person

Posted 14 days ago
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Job 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 Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are currently looking for a Qualified Person to join our team in AbbVie North Dublin. At AbbVie, our Qualified Person (QP) plays a critical role in ensuring the quality, safety, and efficacy of medicinal products. Adhering to EC Directives and Good Manufacturing Practice guidelines, the QP operates within regulatory frameworks and company policies to maintain high standards and resolve challenges impacting product performance. This role is a cornerstone in our commitment to delivering safe and compliant products.
Responsibilities
+ Certify batches of medicinal products per GMP guidelines and ensure compliance with marketing authorizations.
+ Ensure any changes requiring variation to the manufacturing authorisations (MIA and IMP licenses) have been notified and authorised by the relevant authority.
+ Review deviation reports, Product Quality Reviews, Customer Complaints, manage CAPA and investigations, and authorise changes impacting product quality.
+ Collaborate across functional teams to enhance Quality Systems; compile and communicate KPI metrics.
+ Engage in Continuous Professional Development to maintain expertise in QP activities.
+ Support training initiatives, safety compliance, and process improvement efforts within the team.
+ Provide status updates on activities and productivity challenges; seek continuous process improvement.
+ Participate in regulatory, corporate, and customer inspections.
+ Conduct audits of vendors and contract facilities as appropriate.
Qualifications
Educational background satisfying Directive 2001/83/EC for Medicinal Products.
+ At least 5 years of experience in drug product manufacturing, quality assurance, and regulatory interactions.
+ Proficient in EU and FDA cGMPs, regulatory filings, and quality systems management.
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 & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
Qualified Accountant
Posted 2 days ago
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Qualified Mechanic
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Qualified Accountant
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