Hobson Prior are looking for a GCP QA Auditor to join a CRO on a permanent basis located in London.

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 plan, organize, and report internal and external audits.
• Providing support to our audit schedule and esteemed clients.
• Under the supervision of the QA Manager, you will be responsible for conducting GxP audits,
• Identifying trends, identifying corrective actions, and categorizing observations.
• As part of your duties, you'll support initiatives for business improvement with departmental heads.
• Contribute to projects and assist with client audits.
• Provide support and services for pharmaceutical and medical device clinical trials.

Requirements:

• An undergraduate degree in a science subject is required.
• A minimum of 4 years of prior experience auditing to GCP standards, preferably in pharmaceuticals/biotech.
• An understanding of the compliance requirements for clinical trials is essential.
• Hold a valid driver's license.
• Ability to travel approximately 50 percent of the time.
• Operate across Europe, North America, South America, Asia, Africa, and Australasia for audits.

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.