QC Specialist: Analytical Systems & Compliance

Allergan; Dublin; On-site; EUR 50,000 - 70,000; Full time

Job summary

AbbVie in Dublin is seeking a Quality Control professional to build and maintain specifications within ALEXIS LIMS and manage sessions in VelQuest Smartlab, ensuring data integrity and regulatory compliance in a GMP environment.

The candidate should have 3–5 years in Pharmaceutical QC, with strong documentation skills, experience reviewing data, and supporting method validation, change control, SOPs and equipment qualification.

Qualifications

• Bachelor’s degree in Chemistry or a related science field.
• 3–5 years of QC experience in a pharmaceutical setting.
• Strong knowledge of cGMP, USP, and FDA guidance for QC labs.
• Attention to detail in data review and documentation.

Responsibilities

• Build and maintain specifications in the ALEXIS LIMS system.
• Maintain sessions in VelQuest Smartlab.
• Administer laboratory software systems and ensure data integrity.
• Review QC documentation for accuracy and compliance.
• Support change management and prepare validation/docs.
• Draft SOPs and QC documentation; assist with equipment qualification.

Skills

Attention to detail

Quality control

Documentation skills

Education

Bachelor’s Degree in Chemistry or related Science

Tools

ALEXIS LIMS

VelQuest Smartlab

Labware LIMS

Job description

AbbVie in Dublin is seeking a Quality Control professional to build and maintain specifications within ALEXIS LIMS and manage sessions in VelQuest Smartlab, ensuring data integrity and regulatory compliance in a GMP environment.

The candidate should have 3–5 years in Pharmaceutical QC, with strong documentation skills, experience reviewing data, and supporting method validation, change control, SOPs and equipment qualification.