Up to £13.94 per hour
About the Role
Manpower UK is seeking a Sr. QA Technician for a temporary, six-month assignment based in Birmingham, paying up to £13.94 per hour. This role supports a Quality Assurance team within the medical devices and specialty diagnostics sector. Responsibilities centre on batch release activities, including reviewing and verifying Device History Records to confirm compliance with stringent quality and regulatory standards. The position also involves maintaining quality system effectiveness in a highly regulated environment. Candidates should possess strong attention to detail and relevant QA experience. This contract offers an immediate start for the right professional.
Sr QA Technician (Batch Release) - 6 Month Temporary | Birmingham | £13.94 p/h | Immediate Start
The Assignment
We have an immediate requirement for a Sr QA Technician (Batch Release) to join a global organisation operating within the medical devices and specialty diagnostics sector in Birmingham.
This is a 6-month temporary assignment, supporting a busy Quality Assurance team responsible for ensuring compliance, batch release activities and quality system effectiveness within a highly regulated environment.
The assignment is expected to run for 6 months.
What the Work Involves
Working as part of an established Quality Assurance team, your duties will include:
- Reviewing and verifying Device History Records (DHRs) to ensure compliance with quality and regulatory requirements
- Supporting batch review and release activities, ensuring quality events, NCRs and CAPAs are satisfactorily addressed prior to release
- Collaborating with cross-functional teams to resolve quality issues and maintain compliance standards
- Supporting continuous improvement initiatives, KPI reporting, training activities and quality documentation updates
Hours, Shifts andamp; Pay
Shift pattern: Days only, Monday to Friday, 08:30 to 17:00
Pay rate: £13.94 p/h
Pay frequency: Weekly
Holiday pay: Accrued and paid weekly
Overtime: Available
What We Need From You
- Previous experience within a Medical Device, Pharmaceutical, Life Sciences or other regulated manufacturing environment
- Sound knowledge of GxP regulations, particularly GMP, GDP, MDSA
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