Senior QA Specialist – GMP & Lab Systems

AbbVie; Dublin; On-site; EUR 52,000 - 70,000; Full time

Job summary

AbbVie is seeking a Laboratory Quality Control professional in Ireland to build and maintain specifications in LIMS systems and administer laboratory software, ensuring data integrity and regulatory compliance across FDA, GLP, QSR and cGMP standards.

The role requires 3–5 years of QC experience in a pharmaceutical manufacturing setting, with a strong focus on data review and documentation accuracy.

Qualifications

• Bachelor’s Degree or above in Chemistry or related Science.
• 3–5 years relevant Quality Control experience.
• Experience in pharmaceutical manufacturing facility.
• Demonstrate knowledge of cGMP requirements and USP and FDA Guidance Documents relating to QC Laboratory.
• Attention to detail in reviewing data and documentation.

Responsibilities

• Build and maintain specifications in the ALEXIS LIMS system.
• Build and maintain sessions in VelQuest Smartlab.
• Administration of laboratory software systems.
• Maintain data integrity and ensure regulatory compliance (FDA, GLP, QSR, cGMP).
• Draft, review and approve validation/qualification documentation for analytical software.

Skills

Quality Control

GxP Compliance

cGMP

Education

Bachelor's Degree in Chemistry

Job description

AbbVie is seeking a Laboratory Quality Control professional in Ireland to build and maintain specifications in LIMS systems and administer laboratory software, ensuring data integrity and regulatory compliance across FDA, GLP, QSR and cGMP standards.

The role requires 3–5 years of QC experience in a pharmaceutical manufacturing setting, with a strong focus on data review and documentation accuracy.