QA Specialist — 11-Month Hybrid Contract (GMP/Quality)

Morgan McKinley; Dublin; Hybrid; EUR 45,000 - 65,000; Full time

Job summary

Morgan McKinley is seeking a QA Specialist on an 11-month contract with hybrid work in Ireland. The role focuses on data integrity, cGMP compliance, and continued quality improvements across manufacturing records, deviations, CAPAs, and change controls.

The ideal candidate holds a science-related degree and 3–5 years in regulated pharma/biotech environments, with strong analytical, writing, and stakeholder management skills to support product release and quality activities.

Qualifications

• 3–5 years in a regulated pharma/biotech environment.
• Experience with quality systems, deviations, CAPAs, change controls, investigations.
• Knowledge of GMP requirements and quality system standards.
• Experience collaborating with cross-functional teams including Manufacturing, Engineering, Lab, Supply Chain.

Responsibilities

• Ensure ALCOA data integrity for records and data.
• Complete required cGMP training and ensure compliance with regulations.
• Drive cGMP/GDP compliance in day-to-day activities.
• Escalate potential quality violations and aid in resolution.
• Collaborate with QA leads and QPs to resolve quality queries.
• Support introduction of new products for site release.
• Promote processes and procedures for all quality activities.
• Monitor Quality Management Systems and generate performance reports.
• Review and approve manufacturing batch/material documentation.
• Identify improvement opportunities to enhance compliance and efficiency.

Skills

Quality systems

GMP compliance

Analytical thinking

Communication skills

Stakeholder management

Data integrity

Regulatory interpretation

Microsoft Office

Documentation

Problem solving

Education

Bachelor's degree in Science/Engineering/Quality/Pharmaceutical disciplines

Quality Management Certifications desirable

Tools

Electronic quality management systems

Job description

Morgan McKinley is seeking a QA Specialist on an 11-month contract with hybrid work in Ireland. The role focuses on data integrity, cGMP compliance, and continued quality improvements across manufacturing records, deviations, CAPAs, and change controls.

The ideal candidate holds a science-related degree and 3–5 years in regulated pharma/biotech environments, with strong analytical, writing, and stakeholder management skills to support product release and quality activities.