Hobson Prior is looking for a Quality Assurance Specialist to join their team for an exciting opportunity. This role focuses on ensuring quality and compliance within pharmaceutical development activities. You will be a key advisor on Good Manufacturing Practice (GMP) and support the development process to ensure new products meet high-quality standards.

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

Responsibilities:

• Ensure the quality release of manufactured drug products for clinical trials.
• Assist with investigations of deviations and changes in development projects.
• Provide proactive advice to improve GMP quality systems.
• Collaborate with global teams to standardize processes and ways of working.
• Analyze compliance data to enhance quality standards.

Key Skills and Requirements:

• Advanced degree in pharmacy or engineering with a focus on pharmaceuticals.
• Strong understanding of international quality systems and GMP regulations.
• Effective communication skills for internal collaboration.
• Fluent in English, both written and spoken.

For more information, please contact Lisa Venn.

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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