Hobson Prior are in search of a dedicated Principal QA who will provide exemplary quality leadership, invaluable guidance, and meticulous oversight. This position plays a crucial role in transforming the healthcare sector by progressing the development and manufacturing of cutting-edge biopharmaceuticals.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities

• For this role you will be expected to offer high-quality leadership, guidance, and oversight for managing change, deviations, and CAPA processes, along with ensuring compliance with systems and regulations.
• Manage the site program to align with global quality standards.
• Take ownership of the Change and Deviation Management System.
• Coordinate and present site compliance data and management review reports.
• Act as the Business Process owner for Change Management, Trend Analysis, and Activity Planning. Oversee GMP documents and processes related to Change Control, Trend Analysis, Observation Management, and GNP activity planning/tracking.

Requirements

• A degree (BSc, MSc, or PhD) in a science-related field.
• Experience within GMP operations. Specific years of experience are not a requirement, but a solid understanding and practical application of GMP operations are essential.

Apply now

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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