Senior Quality Assurance Specialist

Principal QA Specialist We are partnered with a leading, global CDMO that is looking to hire an experienced senior quality assurance professional for a 12-month contract. You will use your established pharmaceutical experience to take on a subject matter expert function across key quality functions including but not limited to:

• SQC preparation and publishment
• Deviation process tracking and reporting
• Managing deviation Event Category Limits
• Risk management process

Given the nature of the environment, you will have the experience (or at least capability) to deal with a fast paced, commercial manufacturing setting. As this is a maternity cover contract, there are no guarantees for extension although other opportunities may become available. Therefore, this is a great opportunity to get into the business and prove your worth. Please contact Mark Bux-Ryan for further information. Key experience:

• Previous pharmaceutical quality assurance experience in a GMP setting
• Confident and experience across statistical reporting, deviation tracking and quality risk management
• Excellent stakeholder management skills
• Experience and capability of being the subject matter expert in a demanding, client focused, commercial manufacturing setting

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