Hobson Prior is seeking a Quality Associate to join a dedicated team. This position will work with investigational medicinal products, ensuring they meet quality standards before reaching patients. This role will also review clinical batch records to ensure they comply with regulations and work closely with global teams to support the clinical supply chain. This position holds a hybrid working model, 1 day per week is required to be worked in the office based in London, the rest can be worked remote from home.

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

Responsibilities:

• Review and approve production documents to ensure they meet regulatory standards.
• Conduct routine checks of data, procedures, and systems to ensure compliance.
• Communicate and resolve any issues found during audits.
• Work with teams to address and fix any problems identified.

Key Skills and Requirements:

• Experience in the pharmaceutical or chemical industry.
• Understanding of good manufacturing practices (GMP).
• Strong communication skills, both written and verbal.
• Ability to work independently and pay attention to detail.

For more information, please contact Frankie Cunningham.

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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