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.
The Quality Assurance Associate will play a pivotal role in ensuring the highest standards of product quality and compliance within a leading pharmaceutical company.
Our client is a growing business in the pharmaceutical sector and are known for their commitment to quality and innovation, boasting a significant market share and a strong presence in the industry.
This role is based on the outskirts of York, and is integral to the company's mission of delivering excellence in every product.
My client a global pharmaceutical manufacturing company are looking to recruit a Preproduction Quality Assurance Coordinator based in Scotland where you will be responsible for ensuring the integrity of clinical trial supplies packaged at the site.
An exciting opportunity has been created due to company growth.
Day to day duties include
Generating clinical trial packaging documentation to meet the company, Client, Study and Regulatory requirements.
Rocasa Consulting is looking for a Head of Quality Assurance and Service Improvement to join the team of a vibrant social housing company at their Bristol's branch.
The pay rate will be £35.84 per hour (equivalent of £250.88 per day) - based on 40 hours per week.
The contract will start in July and run until the end of November.
We have an exciting opportunity for a QC / Testing Operative in the pharmaceutical industry.
If you're a recent science graduate passionate about quality control and testing, this role is perfect for you.
Join a leading pharmaceutical company on a temporary basis, where you'll play a crucial role in ensuring the highest quality standards for pharmaceutical products.
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.