Quality Manager
Posted a day ago
- Lee Moor, Devon
- Any
- External
- Expires In 3 months
Quality Manager - Devon - Up to £60,000 pa + Benefits - Ref 1816
I am currently recruiting for a Quality Manager to work for a multi-national manufacturing organisation. Salary up to £60,000 pa + Benefits.
Devon
Up to £60,000 pa + benefits
You will be responsible for leading the site quality function. To manage successful delivery of the Quality strategy to deliver the corporate goals and objectives. To assure necessary compliance requirements through the Quality Management System including continuous improvements, CAPA management, document management, quality planning, internal and external audits, validation, risk management, and continuous Quality Management Review.
Requirements:
Must have experience maintaining, updating & improving QMS
Experience working within the medical device, pharmaceutical industry with ISO13485 knowledge (preferred but can also look at Automotive, Aerospace or ISO9001)
Ability to deliver change management
Manage internal audits + host site audits
Ability to support QMS deliverables
Desired:
Knowledge of applicable regulations and standards related to medical devices internationally (ISO 13485, MDR, MDD, MDSAP)
This is a fantastic opportunity for a Quality Manager to work for a leader within their field where the work is continuously varied keeping you engaged and challenged.
This is an immediate requirement so if you have the required skills and experience then please get in touch ASAP with an up to date copy of your CV. Either apply direct or contact David on 01183 366 100.
TPBN1_UKTJ
I am currently recruiting for a Quality Manager to work for a multi-national manufacturing organisation. Salary up to £60,000 pa + Benefits.
Devon
Up to £60,000 pa + benefits
You will be responsible for leading the site quality function. To manage successful delivery of the Quality strategy to deliver the corporate goals and objectives. To assure necessary compliance requirements through the Quality Management System including continuous improvements, CAPA management, document management, quality planning, internal and external audits, validation, risk management, and continuous Quality Management Review.
Requirements:
Must have experience maintaining, updating & improving QMS
Experience working within the medical device, pharmaceutical industry with ISO13485 knowledge (preferred but can also look at Automotive, Aerospace or ISO9001)
Ability to deliver change management
Manage internal audits + host site audits
Ability to support QMS deliverables
Desired:
Knowledge of applicable regulations and standards related to medical devices internationally (ISO 13485, MDR, MDD, MDSAP)
This is a fantastic opportunity for a Quality Manager to work for a leader within their field where the work is continuously varied keeping you engaged and challenged.
This is an immediate requirement so if you have the required skills and experience then please get in touch ASAP with an up to date copy of your CV. Either apply direct or contact David on 01183 366 100.
TPBN1_UKTJ