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
Quality, assurance, contract, manufacturing, PQR, deviation, CAPA, statistic, metrics, SQC, QRM, risk, management, QA