As a Quality Administrator, you will play a vital role in maintaining our standards of excellence by managing client complaints, non-conformances, and compliance activities.
To monitor the Laboratory quality system compliance and effectiveness through planned audits and independent process control checks to ensure that our products comply with food safety legislation, meet the technical and quality specification and are manufactured at best cost.
To ensure customer expectations are met and exceeded at every level.
Job Context
Reporting directly to Technical team leader for day to day operations, working alongside factory colleagues and key disciplines i.e.
Posted by Newton Colmore Consulting Ltd • £35K/yr to £50K/yr
We are currently looking for a Quality Engineer for a growing start-up Medical Devices organisation.
You will be reporting into the Quality Assurance Manager and collaborate various Medical Devices experts, including Mechanical Engineers, Physicists, Electronics Engineers, Software Engineers, and other professionals.
The company is developing a medical device that is changing the lives of thousands of people and was recently covered in some news articles due to the impressive detail of their work.
We are currently recruiting for one of the largest global pharmaceutical companies, recruiting for a Quality Assurance Officer to support day-to-day QA activities associated with the effective running of the site QMS supporting batch release.
Our client, a global manufacturer and supplier of flavourings, extracts, and essences, is seeking a talented Quality Control Supervisor to join their team !
Reporting to a Quality Manager you will provide day-to-day assistance for commercial QA activities associated with effective running of the site QMS supporting batch release.
SRG are working with a global pharmaceutical company who are seeking a QA officer to join their Marlow site.
The QA Officer will ensure assigned tasks are performed in a timely manner to meet internal standards and all associated international GMP/GDP requirements.
My global pharmaceutical client, based in Buckinghamshire, are looking for a Spanish Speaking Post Market QA Analyst to join their team on a 12-month basis.
The perfect candidate will be a good communicator with good written and spoken language in English and Spanish.