As laboratory quality (QC) coordinator you will manage the quality process - planning and supervising the lab work, testing raw materials, plating for tests, quality checks on flasks, vessels, after packing and shelf life.
As a QC / Quality Laboratory Coordinator you will deputise in managing the work within the laboratory for a global organisation to ensure the tasks are completed and support technicians.
Key Responsibilities
Manage the quality control process for all products manufactured.
Maintaining quality documentation to required standard, tracking, and updating documents as required.
Develop a high level of communication and engagement with various teams, to improve quality management system.
General
Reports to Operations Director Interfaces with Project Leader / project team members / HR Department Job summary: Responsible for the coordination of relevant quality documentation and preparation of various audits.
Quality Coordinator / Near Lancing / Up to £40k DoE
As a Quality Coordinator, you will play a vital role in ensuring the seamless launch of new products and maintaining high-quality standards throughout the manufacturing process.
Are you looking for a brand new opportunity within engineering & manufacturing quality?
Our client, a leading business in the manufacturing sector for what they manufacture is seeking a dedicated and experienced Quality & Compliance Coordinator to join their team.
With a commitment to excellence and sustainability, our client operates at the forefront of technology, ensuring compliance with industry standards and regulations.
Role Overview
Reporting directly to the Head of Engineering, the Quality & Compliance Coordinator will play a pivotal role in ensuring adherence to quality, environmental, and safety standards across all company operations.
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.
Butler Rose are delighted to be working on an exclusive basis with a business in the Welllington area who have a current requirement for a Quality Coordinator.
Ensuring manufactured products repairs have been correctly processed through internal business functions to meet high standards of quality.
The tole is wide ranging in scope, but will primarily ensure that the internal QMS processes and procedures comply with the requirements of business standard ISO9001 and the companies customer requirements.