Principal QA Specialist

​rincipal 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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