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.
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
* 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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