The purpose of the Quality Assurance Advisor is to complete regular quality assurance activity on the Flexible Recruitment processes, focusing on the end-to-end order to invoice process of flexible resource, provided by Angard.
Through regular checking and governance of the processes you will identify areas of non-compliance and liaise with the business and our external providers to rectify process failures and recover any financial loss.
You will also support the development of systems, processes and policies as we develop this side of the team and create a robust governance framework for Flexible Recruitment.
Our reputable fashion client are currently looking for an experienced Head of Quality to join their team on a fixed term basis, this role is to cover maternity leave.
We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics.
We operate at impressive scale, producing over 1.7 billion packs of medicine and 767 million vaccine doses in 2021.
My client are an expanding pharmaceutical manufacturing organisation seeking a highly motivated and experienced Quality Assurance Manager to join their sterile manufacturing facility.
Contract until end of Dec 2024 (3 days a week)
Salary Negotiable dependent on experience plus benefits
Responsible for the environmental and H&S control of assembly, integration & test activities in accordance with the appropriate standards.
Ensure conformity of production and test operations within the Cleanroom in accordance with Plans, Processes and Procedures for Space Equipment production, to approved quality standards in particular ECSS-Q-ST-70-08, 28 & 38.
Responsible and accountable for the correct "as built as design" validation.
Our client is a well-established organization based in the Birkenhead/Merseyside area, and actively seeking to recruit an experienced QC Technician to join their Quality department on a three-month contract.
Ideally, the candidate would be available to work from 5 pm to 10 pm, though they are also open to considering someone who can work a 1 pm to 10 pm shift.
The role holder is responsible for working cross-functionally and reviewing and compiling batch specific documentation and data for batch release, ensuring compliance with licensed and cGMP requirements, escalation of potential issues, and timely submission of LRPs/release of batches in order to meet supply demands.
12 Month Contract
Batch Release Co-ordinator - £18.00 Based on Site in Liverpool.
The role holder will be required to supervise the activities of personnel carrying out works for UNS (which includes employees, ASW and contract workers) on a day to day basis to ensure that all activities are executed in a safe, cost effective and reliable manner inline with legislative and company procedures.
The role objective is to ensure that construction, demolition and decommissioning works are carried out to specification and by safe working methods.
The role holder shall work closely with the wider UNS team to support the characterisation, monitoring and transfer of waste.