Quality Manager - Old Dalby, United Kingdom - Executive Network Group

Tom O´Connor

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Tom O´Connor

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Description

The Executive Network Group is currently recruiting for a Quality Manager near Melton Mowbray for a fantastic client in the Medical Device/Pharmaceutical sector in what is an incredibly exciting opportunity.

This role is responsible for the maintenance and co-ordination of the Quality Systems whilst supporting the business in ensuring that it operates in compliance with all relevant quality and regulatory standards.


Job Title:
Quality Manager

Location - Leicestershire (North of Melton Mowbray)
Salary - £40,000 - £45,000

The successful Quality Manager will be responsible for the following:

  • Conducts regular reviews of all quality critical documents, systems and procedures to ensure any required changes are made.
  • Manage, motivate, development, mentoring and coaching the Quality team to ensure performance and productivity is at least to the expected standards
  • Supports the Manufacturing Quality Manager to ensure quality procedures can be implemented appropriately.
  • Support the Senior Quality Manager in ensuring compliance to GDP
  • Actively looks to improve the Quality Management System in line with new regulatory guidelines, and industry best practice.
  • Quality Lead on site projects/ change controls to drive new projects initiative forwards to promote right first time.
  • Responsible for change control, planned deviations, Quality Risk assessments, re
- work processes

  • Responsible for Validation and verification of equipment, processes, and new products
  • Maintains all quality critical documents eg Quality manuals, SOPs, Quality Policies, Audit Reports, through the support of other team members
  • Responsible for Quality Investigation Reports and deviations including the CAPA plan.

The successful Quality Manager will have the following skills & experience:

-
Essential:


  • Extensive Quality Management experience within a regulated healthcare environment
  • Excellent understanding of regulations supporting healthcare product development, ie GMP, GDP, Medical Device, ISO 9001, ISO 1348
  • Familiar with Product Development Lifecycle and its processes.
  • To be a proactive problem solver
  • To be able to work as part of a team and develop self and others
  • To share their knowledge and experience with others
  • Experience in conducting audits internally and externally

Desirable:


  • Knowledge of HACCP, BRC.
  • Experience of hosting internal and external audits from regulatory bodies.
  • Experience in hosting audits from retail customers.

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