Posted by Science Solutions Recruitment Ltd • £16.31/hr to £24.05/hr
To be considered for this QC Analyst you will have previous industrial experience as a technician or qc analyst within the manufacturing sector, skilled in performing a range of testing techniques.
As a QC Analyst you will be responsible for providing expert analysis to support manufacturing processes ensuring compliance to all specifications and standards are maintained.
You will be performing testing and analysis of raw materials, in-process testing and final products, as well as evaluating and validating data and calibration and maintenance of various equipment.
Posted by Central Employment Agency (North East) Limited • £23K/yr to £27K/yr
The opportunity will be working in the Quality Assurance team creating, monitoring and implementing Quality systems that are required in a pharmaceutical manufacturer.
This is an excellent opportunity to join a leading business, understanding the importance of quality, compliance and the systems that underpin and create the foundations for all regulatory requirements.
Central Employment is delighted to present an opportunity to work in a global pharmaceutical business.
This opportunity is for a Senior QC Analyst Validation to join the QC Technical Services Team on a contract basis.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
The duration of the contract will be 23 months with a start date in September 2024.
We are currently looking for Quality Controller for client based in Headcorn.
Reporting to the Technical Supervisor
Testing and inspection of materials and processes from intake to final dispatch, ensuring all specifications are met and exceptions are reported and acted upon in a timely manner.
Posted by Randstad Delivery (GBS) • £22/hr to £27/hr
Position Overview
We are seeking an experienced and highly motivated Product Quality Assurance Manager to lead our Quality Assurance team.
The successful candidate will oversee the compliance audit of manufacturing and quality control records, manage material inspections, and take full accountability for the release of finished in-vitro diagnostic products.
This leadership role is crucial in ensuring the independent approval of raw materials, process intermediates, and finished products in line with cGMP standards.