SRG - QA Officer

Job Title:

QA Officer

Category:

Technical roles

Closing Date:

30/09/2024

SRG are working with a global name in the pharmaceutical industry to help them find a QA Officer for a 12 month FTC.

If you have Quality Assurance (QA) experience from a GMP environment then this could be a great next step for you.

The company offer an excellent benefits package and flexible working.

The Role:

• Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures and Analytical Procedures.
• Participate in quality related investigations, assist in the development and approval of effective CAPA in order to resolve production, audit and customer issues.
• Identify and escalate any identified cGMP areas of concern.
• Participate in validation activities including approval of protocols and reports for analytical methods, manufacturing processes, analytical / production / packaging equipment and cleaning procedures
• Participate in the audits of suppliers, production and support functions as required.
• Be involved in the preparation for MHRA/FDA and other regulatory body audits.
• Review the relevant documentation relating to incoming raw materials and perform the disposition activities as required.
• Reviewing manufacturing, laboratory and associated documentation prior to performing the relevant disposition of final products. Where potential issues exist, these are to be highlighted to the QA manager.
• Act as the QA representative for the introduction of new products, being a key member of the multi-functional team including R&D, QC and manufacturing thus ensuring that all cGMP documents are appropriate and all cGMP requirements are satisfied.

Requirements:

• Degree in a relevant scientific, engineering or business discipline and/or relevant industry experience
• Several years’ experience within Quality Assurance working to GMP guidelines
• Experience of working within a Quality Management System e.g. completing or reviewing QMS documentation (SOPs/Deviations /Investigations /CAPA)
• Experience of preparing and assisting in external audits with regulatory bodies such as FDA and MHRA
• Organised and attention to detail
• Strong communication skills across all levels

If you meet the above requirements, please send a CV to emma.laurenson@srgtalent.com