SRG is currently working exclusively with a highly successful & award winning, CDMO based in Greater Manchester. Growing rapidly, the business specialises in taking products from discovery, all the way through early-stage trials, and to approval. They are now looking for an experienced QA Officer to join the quality team, and support GMP operations.
The Role:
Working alongside the QA Manager you will be responsible for supporting the day-to-day QMS activities, ensuring the sites ongoing compliance with quality / regulatory standards and industry best practises.
Key duties will include:
* Assessing & implementing CAPAs & change controls.
* Creating, reviewing, approving & managing quality documentation such as specification, SOPs, & protocols.
* Supporting QP release activities.
Requirements:
* A degree or higher qualification in a relevant Scientific discipline
* Recent QA experience within a Pharmaceutical GMP environment
* Experience with Investigational Medicinal Products (IMPs) would be advantageous
* Excellent communication skills and a keen eye for detail
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