Hobson Prior are in search for a permanent QA Compliance Officer to join a leading organisation focused on the development and manufacturing of biopharmaceuticals.

Job Responsibilities:

• Support the co-ordination and planning of the IPT workload, ensuring Quality matters are considered and acted upon in a compliant fashion.
• Actively participate in Quality investigations, change controls and risk assessments associated with the IPT.
• Review and approve key documents associated to the IPT.
• Perform review of batch manufacturing records and release relevant material for the next stage of manufacture.
• Provide appropriate QA oversight of manufacturing and testing processes within the IPT to support the business.
• To participate in the data gathering/review for the quarterly trending reports and annual PQR for the related stage of manufacture.
• To promote and enforce data integrity compliance within the IPT.
• If relevant to the specific IPT, to provide review and approval support to EM investigations, smoke visualisation studies, product complaint investigations.

Key Skills:

• Strong organisation skills.
• Excellent communication skills.

Requirements:

• Experience in operating quality systems in a GMP environment with proven evidence of encountering a wide range of situations
• Experience of preparing and providing accurate documents and reports in a timely fashion
• Practical experience in GMP Biopharmaceutical manufacture

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.