Pharma QA Specialist - Hybrid 11-Month Contract

PE Global; Carlow; Hybrid; EUR 52,000 - 65,000; Full time

Job summary

PE Global is currently recruiting a QA Specialist for our client in Carlow. This 11-month initial contract offers hybrid work with 2–3 days on site. The role focuses on quality assurance activities, data integrity (ALCOA), and cGMP compliance across QA systems.

Ideal candidates have 3–5 years in a regulated pharma/manufacturing environment and a related Bachelor’s degree. Please note visa sponsorship is not available for this position.

Qualifications

• 3–5 years in a regulated pharmaceutical/biotech/medical device environment.
• Experience with Quality Systems and Compliance functions incl. deviations, CAPAs, change controls, investigations, complaints.
• Knowledge of GMP requirements and quality system standards.
• Experience collaborating with cross-functional teams (Manufacturing, Engineering, Lab, Supply Chain).

Responsibilities

• Ensure data integrity and ALCOA principles in day-to-day activities.
• Participate in cGMP training and ensure compliance with corporate regulations.
• Drive cGMP/GDP compliance in daily activities and escalate potential violations.
• Liaise with QA Leads/QP to resolve quality-related queries.
• Provide QA support for new products and site release activities.
• Develop and monitor quality processes and generate performance reports.
• Review manufacturing batch/material documentation and electronic batch records.
• Support site quality initiatives to improve compliance and efficiency.

Skills

Quality Management Systems

GMP compliance

Analytical problem-solving

Written and verbal communication

Multitasking

Stakeholder management

Attention to detail

Regulatory interpretation

Continuous improvement

Data integrity (ALCOA)

Education

Bachelor's degree in Science/Engineering/Quality/Pharmaceuticals

Tools

Microsoft Office

Electronic Quality Management System

Job description

PE Global is currently recruiting a QA Specialist for our client in Carlow. This 11-month initial contract offers hybrid work with 2–3 days on site. The role focuses on quality assurance activities, data integrity (ALCOA), and cGMP compliance across QA systems.

Ideal candidates have 3–5 years in a regulated pharma/manufacturing environment and a related Bachelor’s degree. Please note visa sponsorship is not available for this position.