GROUP QUALITY PROCESS MANAGER
Do you have extensive experience in Quality Processes and Process Improvement?
Do you enjoy travelling in a varied, challenging career?
As a Group Quality Process Manager you will work closely with several Quality Site Managers across the UK and Europe to standardise and improve the Quality Management System processes.
You will manage and set up the group function within Quality.
You will ensure compliance to FDA, ISO 13485, ISO 14971, MDD 93/42/EEC.
You will travel regularly to European sites to liaise with Quality Managers and implement new processes.
Skills and Experience:
Minimum of 10 years' experience within Medical Devices or Pharmaceuticals in a similar position.
Working knowledge of ISO 13485, FDA, MDD 93/42/EEC
Significant process improvement experience
Ability to analyse and interpret standards, technical documents, professional journals and government guidance/regulation documents.
Educated to degree level or significant relevant experience.
Salary circa £75k (dependent on experience)
Permanent contract, Full Time
Location: Cheshire + European travel
CALL NOW on 0161 839 5353 or email Jacob Golding - firstname.lastname@example.org