Adecco working in collaboration with Bentley Motors, an esteemed player in the Automotive sector, is seeking a talented UX/UI Engineer to join their team on a temporary contract for 6 months.
Are you ready to combine luxury and progressive technology to shape the future of the automotive industry?
This is an exhilarating opportunity to be part of Bentley Motors' thrilling transformational phase.
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.
Posted by Randstad Delivery (GBS) • £22/hr to £27/hr
Main Purpose of Job
In this role, you will be responsible for implementing and maintaining the site's Quality Management System (QMS) to ensure compliance with industry standards.
We are seeking a highly motivated and skilled Manager of Quality Systems to join our team in Dundee, Scotland.
This position plays a crucial role in driving quality improvements and supporting diagnostic testing, which provides key insights into disease treatment and management.
We are looking for an innovative, experienced, and talented senior software engineer who will work closely with business unit and development team to develop new system capabilities as defined within the technical/ functional specifications
Key Responsibilities
Handle coding, debugging, and documentation, as well working closely with SRE team.
Responsible for leading projects, designing system solutions, developing custom applications, and modifying existing applications to meet distinct and changing business requirements.
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.