QA Specialist — 12‑Month Contract (Connaught Region, Ireland)

📋 Role Summary

The QA Specialist will act as the prime quality contact at-site and liaise with external stakeholders. You’ll manage key quality processes—including URS development, change control, protocols, and pre- & post‑approval activities—while collaborating in cross-functional teams.

🔧 Key Responsibilities

• Serve as the main QA contact at the site and within external quality working groups.
• Oversee QA deliverables: URS, protocols, reports, change controls, and approval sign-offs.
• Participate in cross-functional initiatives as a QA subject-matter expert.
• Coordinate and attend Quality Working Group meetings, ensuring alignment with cGMP standards.

🎯 Qualifications & Requirements

• Proven QA experience in a biopharmaceutical or similar regulated environment.
• Strong, demonstrable knowledge of cGMP regulations.
• Excellent organization, planning, and time-management skills.
• Self-starter with flexibility to thrive in a fast-paced, dynamic setting.
• Exceptional attention to detail.
• Proactive communication style and effective cross-functional collaboration.
• Motivated team player with stakeholder-focused attitude.

🎁 Benefits & Contract Details

• 12‑month contract with a biopharma leader in the Connaught region.
• Opportunity to contribute to a growing site and quality infrastructure.
• Collaborative and supportive working environment.
• Fully remote support not guaranteed—site-based presence expected.

✅ Application Details

• Salary Range: Not disclosed
• Application Deadline: July 31, 2025
• How to Apply: Submit your CV and cover letter via this link: Apply Now