Do you have a strong understanding of quality assurance and GMP compliance? This role is your perfect next step in your career… apply today!

Hobson Prior is seeking a dedicated IMP Quality Manager Specialist to ensure that investigational medicines are produced safely and effectively. You will be part of a dynamic team focused on maintaining high standards and compliance with regulations.

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

Responsibilities:

• Act as a representative for quality assurance in the production of investigational medicines.
• Ensure manufacturing and testing processes meet quality standards.
• Review and approve important documents and reports related to production.
• Conduct inspections in manufacturing facilities and labs.
• Report directly to senior quality assurance leaders.

Key Skills and Requirements:

• Degree in Life Sciences or similar field.
• Experience in the pharmaceutical industry, particularly in quality assurance and GMP environments.
• Familiarity with manufacturing and quality control of injectable medicines.
• Strong knowledge of GMP regulations and quality standards.
• Experience with managing discrepancies, changes, and using management systems like SAP and LIMS.
• Proficient in English and German communication.
• Ability to learn quickly, work well in teams, and manage multiple tasks efficiently.

For more information, please contact Frankie Cunningham.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' 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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