This job is no longer available
Salary £25,000 -£27,000
A global organisation is currently recruiting for a Quality Assurance and Regulatory Affairs Advisor to be based in their site in the Southwest. This worldwide organisation provides bespoke solutions for the Medical Device industry for improvement treatments.
This fantastic organisation complies with high Quality standards and regulatory that continue growth and development within the company. They are looking for someone to plan and deliver their work on time, providing solutions to problems encountered. As a Quality Assurance advisor you will be responsible that all Quality systems are maintained and established along with accurate decisions made within scope of the role.
You must have a minimum of 2 years' experience in Quality Assurance AND Regulatory Affairs and proven ability to work a part of a team, someone who has a working knowledge of Medical Device 13485 or manufacturing organisation would be an advantage. As a Quality Assurance Advisor you will have the responsibility of complaint handling, internal audits, QC Specifications, ISO9001, control of quality related documents, management of the inspection of raw materials, work in progress along with other task necessary.
The working environment and quality of work within the business are of the highest order and the successful individual can expect to be well rewarded both with their career development. Subsequently they are looking for someone to come in and be a good communicator and a great influencer to the business proving solution. This is a new role that is growing rapidly; this position would potentially suit a candidate looking for a new challenge along with demonstrating their abilities.
If you want to be a part of this exciting opportunity, Please contact Ekta Multani, Medical Devices Recruitment consultant at Paramount Recruitment on 0121 616 3474.
Key Words: Quality Assurance, Quality Engineer, Quality Advisor, Medical Devices, ISO 13485, Quality Systems, Regualtory Affairs CAPA, Medical Device Directive, QMS, 21 CFR part 820, Quality Control, Management, Six Sigma, LEAN, GMP, Quality Engineering Manager, ISO 9001
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