Quality Assurance officer - #1785655
TieTalent
Date: 7 hours ago
City: Manchester
Contract type: Full time
Work schedule: Full day
About
Quality Assurance Officer
Greater Manchester
£30,000 - £35,000
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
Investigating & Addressing deviations Assessing & implementing CAPAs & change controls. Supporting continuous improvement activities 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 detailCarbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy
Quality Assurance Officer
Greater Manchester
£30,000 - £35,000
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
Investigating & Addressing deviations Assessing & implementing CAPAs & change controls. Supporting continuous improvement activities 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 detailCarbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy
- Manchester, England
- QA
- QA Test Automation
- English
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