Pharma QA Specialist – cGMP & QC Systems

Allergan; Dublin; Hybrid; EUR 65,000 - 90,000; Full time

Job summary

AbbVie in Dublin is seeking a Quality Control professional to manage LIMS systems, oversight of analytical methods, and data integrity across QC processes. The role involves ensuring compliance with cGMP and FDA guidance while supporting instrument qualification and change management.

The successful candidate will maintain documentation, draft SOPs, and contribute to continuous process improvements within a pharmaceutical manufacturing setting.

Qualifications

• Bachelor’s degree in Chemistry or related science with strong analytical background.
• 3–5 years of relevant Quality Control experience in a pharmaceutical manufacturing setting.
• Knowledge of cGMP, USP and FDA Guidance documents relevant to QC laboratories.

Responsibilities

• Build and maintain specifications in LIMS systems and ensure data integrity.
• Review QC documentation and support instrument qualification and calibration.
• Draft, review and approve analytical methods, SOPs and related documentation.
• Perform routine audits of QC data and support continuous process improvement.

Education

Bachelor’s Degree or above in Chemistry or related Science Abbvie

Tools

ALEXIS LIMS

VelQuest Smartlab

Labware LIMS

Job description

AbbVie in Dublin is seeking a Quality Control professional to manage LIMS systems, oversight of analytical methods, and data integrity across QC processes. The role involves ensuring compliance with cGMP and FDA guidance while supporting instrument qualification and change management.

The successful candidate will maintain documentation, draft SOPs, and contribute to continuous process improvements within a pharmaceutical manufacturing setting.