Job Ref: 215641149

Date: 2022-01-24 16:24:23

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The company

We are currently working with a well established client looking to expand their quality team. This is a market leading, global Medical Device company that is present in 40 countries and have a wide range of medical device products.

With a work environment focused on developing and empowering its employees, there is a genuine chance to grow and progress in the business.

About the role

This mainly office-based position reports to the Production Supervisor, and will work within the quality team to implement and maintain QA processes in the production area.

The role involves working with QMS documentation and processes, investigating non-conformances, and managing SOPs amongst other QA tasks.

This position would suit an early career QA professional looking to broaden their experience in the medical device industry, or someone looking to move from a regulated production role into QA.

Key competencies and experience

– Previous production experience within a regulated manufacturing industry (medical devices or pharmaceutical would be preferred but this is flexible)

– Experience using QMS systems

– ISO13485 or ISO9001 experience preferred

– Internal auditing experience or understanding would beneficial (conducting or participating)

– Good communication skills

– Great eye for detail

Keywords:

QA, quality, assurance, medical, devices, 13485, ISO, audit, CAPA, document, documentation, investigation, complaint, deviation, supplier, external, QMS, manufacturing, SOP, process, change, controls

Harris Lord is acting as a recruitment agency for this role

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