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SciPro are partnered with a rare disease focused clinical-stage biopharmaceutical company gearing up for commercialisation, to support the search for a QA Specialist based in Ireland. This is an exciting opportunity to join a small, agile team at a pivotal moment of growth ensuring quality and compliance as the company advances toward its next stage of evolution.
Working within a fully virtual environment, the QA Specialist will support the Quality Director in maintaining and improving the Quality Management System, overseeing GMP/GDP vendors, and ensuring operational excellence across the organisation. This is a hands-on role ideal for a self-starter who thrives in a fast-moving, entrepreneurial setting.
Key Responsibilities
Oversee and maintain the Quality Management System (QMS), ensuring compliance with GMP and GDP standards.
Update and manage SOPs and QA documentation.
Monitor vendor performance — ensuring change controls, CAPAs, and deviations are tracked and closed on time.
Support continuous improvement initiatives.
Key Requirements
Solid background in GMP/GDP within a biotech, pharmaceutical, or CDMO environment.
Hands-on experience with QMS management, vendor oversight, and system implementation.
Strong documentation, organisation, and communication skills.
Self-driven, pragmatic, and adaptable; comfortable in a small, virtual, and fast-evolving organisation. Able to work autonomously while collaborating closely with leadership
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Looking for your next career move? Join a top company hiring Quality Assurance Specialist job near me in Ireland! This is your chance to work on exciting projects, grow professionally, and enjoy a rewarding career with competitive pay and excellent benefits. Whether you're an experienced professional or looking to take the next step, this role offers the perfect opportunity to enhance your skills and make an impact. Don’t miss out—apply today via Vita CV and take your career to the next level!
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