Hobson Prior are looking for a QA Auditor to join a leading global biopharmaceutical company that has been inventing for life for more than a century.

Job Responsibilities:

• Accountable to conduct routine reviews of data, information, procedures, batch records to ensure the compliance with SOPS and GMPs and worldwide regulations.
• Communicates and resolves review comments with client areas. Under supervision, or as part of a team, perform self-inspections of assigned areas or systems to assess compliance with regulatory and Company standards.
• Review and approve production and analytical documentation accompanying the release of API, Safety Assessment or clinical supply lots (bulk and packaged) to ensure conformance to appropriate regulatory requirements.
• Issue reports summarizing deficiencies and work with areas to execute remedial action. Notify appropriate management of inspection result.
• Drives improvement initiatives and participates in meetings with peers to advance performance.
• Works with moderate work direction and is skilled and knowledgeable to the position.

Requirements:

• GMP experience.
• Prior experience of SOP reviewing.
• API product exposure.
• Batch record review.
• Good documentation practice.

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back 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.