Quality Specialist (Quality Management Systems)

Leeds, West Yorkshire
Up to £28135 per annum + .
12 Mar 2018
09 Apr 2018
Manpower UK
Job Type
An exciting opportunity has arisen to join a world leading global organisation, our Global FMCG Client, are currently seeking a Quality Specialist (Quality Management Systems) based at their facility in Seacroft, Leeds. This is a full time temporary role for a period of 6 months working a 37.5 hour week. This role is paying £28,135.

Main Job Purpose:
The Quality Specialist works within the Product Group organization focused on factory operations, implementing, executing, improving and providing technical quality support to manufacturing sites for Quality Management System (QMS) compliance, innovation execution, quality risk management and quality improvement.

Key Responsibilities:
Supports the organization's QMS conform to ISO13485 requirements
Supports the Quality Management System development for Medical Devices in Europe
Contributes with the devising and establishment of company's Medical Device quality procedures, standards and records
Implement the relevant procedures described in the Medical Device QMS
Ensure that all necessary systems and procedures are in place to satisfy ISO13485 requirements and audits
Introduce new systems and procedures where appropriate
Train others in all aspects of the quality system and application of procedures
Verify closure of non-conformities with Certification Bodies
Support the implementation of Communication/Data Tools to ensure QMS Program and improve the knowledge management approach in the business
Make suggestions for changes and improvements and how to implement them
Interact with different functions across the business at different levels

Experience Required:
University degree in Technical or Science subject (e.g. Biology, Chemistry, Engineering, Food Science or Microbiology).
Appropriate functional business experience in manufacturing, quality, R&D or supply chain
Quality Management System knowledge/experience
Experience of writing QMS procedures

ISO13485 or ISO 90001 experience/knowledge
Medical Device experience

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