As a Senior QA, you will be working in a fast paced, delivery focused environment, playing a critical role in helping a fast-growing company to define and establish its automated test processes and overall quality strategy for several cutting-edge products.
We have an exciting opportunity for a highly technical Senior QA to join a rapidly expanding Sports Analytics company based in London Bridge.
The Senior Regulatory Officer is responsible to deliver end to end regulatory package under ODM-Distributor scheme in compliance with an established quality management system, overseeing initial compilation of design control evidences, supplier management, incoming inspection and product release process, product submission, post-market surveillance, vigilance and associated reporting
SRG is working with a leading Biotechnology company based in the Edinburgh area who are looking for a Senior Regulatory Compliance Officer to join their team on a permanent basis.
The Role
Preparing and compiling regulatory documentation, coordinating and executing regulatory submission in compliance with ISO13485, IVD 2017/746 Regulation, FDA 21 Code of Federal Regulations (CFRs), Medical Device Approvals (510(k)), and other country requirements as appropriate.
Our client, a trusted partner of the UK Ministry of Defence, is seeking an experienced Quality Engineer to provide guidance and support in managing non-conformance issues.
The Quality Engineer will work closely with the manufacturing teams and other relevant departments to facilitate Non-conformance Management and provide guidance on Quality Engineering Issues.
The selected candidate will be responsible for ensuring that relevant fault analysis is conducted during the manufacturing process and that appropriate corrective actions are taken to mitigate any identified issues.
Looking for Quality control Technicians to join the FPS Client team.
Receiving Inspection experience is a must, as well as a working knowledge of Microsoft products and the ability to interpret specifications and drawings.
Cpl Life Sciences are partnering with a global pharmaceutical company to support QC laboratory electronic systems (e.g., LIMS, CDS) as a Senior QC Systems Technical Specialist, this role involves maintaining master data, troubleshooting issues, implementing system improvements, and ensuring compliance with SOPs, GMP, and Data Integrity guidelines.
Key Responsibilities
Support the operation, maintenance, and improvements of the QC electronic systems.
Create/maintain master data for QC electronic systems.
Posted by Randstad Construction & Property • £15/hr to £17/hr
Position Overview
You will be doing quality control Inspections on Medical devices Vital sign monitors, you will play a critical role in our supply chain and quality control processes.
Your primary responsibility will be to ensure the accuracy of incoming finished products, verifying their quality, and conducting inspections to maintain our high standards.