Quality Assurance Specialist

Overview

Join a leading biopharmaceutical company in Limerick as a Quality Assurance Specialist on a 12-month contract. This role involves ensuring quality standards across manufacturing and related areas in a high-tech facility creating innovative treatments for serious diseases.

Key Responsibilities

• Ensure comprehensive compliance of quality protocols encompassing manufacturing, quality systems, quality control, validation, facilities, and materials management at the site.
• Collaborate with multidisciplinary teams to address issues, conduct investigations, and sustain compliance.
• Review and authorize documents such as failure investigations, CAPA reports, SOPs, GxP documentation, and change controls.
• Lead and support root cause analyses and oversee CAPA implementation to prevent issue recurrence as a quality approval authority.
• Evaluate procedures, policies, and instructions related to quality systems for adherence to company standards and international regulatory requirements.

Candidate Profile

• Holds a Bachelor’s degree in a scientific discipline or related field with at least 2 years of relevant pharmaceutical or related industry experience, or an equivalent mix of education and experience.
• Demonstrates a strong background in Quality Assurance within pharmaceutical manufacturing in compliance with GMP.

Additional Information

• Contract duration: 12 months
• Location: Onsite at Limerick, Ireland
• Eligibility: Must be entitled to work in Ireland, holding Stamp 1G or Stamp 4 visa status.
• Experience required: Minimum 5 years in pharmaceutical or biotechnology sectors preferred.

Why Join

• Work on-site with prominent biopharma organizations on impactful projects.
• Receive structured onboarding ensuring readiness from day one.
• Access continuous support and regular engagement throughout the assignment.
• Become part of a wider consultant network and enjoy dedicated team assistance for project and contract navigation.