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Job Details

Quality Manager - West Midlands

Company: X4 Group
Location: West Midlands
Reference: RR 784 WMQM
Closing Date: 16 Jun 17
Type: Permanent
Salary (£): 40,000 - 60,000
Benefits:

Job Summary:

Quality Manager / QA RA Manager / Quality and Regulatory Manager Location: West Midlands, South BirminghamSalary: £35,000 - £45,000 DOE potential to be flexible I am currently working with a Medical Device Manufacturing Company who are seeking a Quality & Regulatory Manager to join their team on a permanent basis. This is a small company who are working on a range of developing products. It is not essential to have Regulatory experience. ...

Requirements:

Quality Manager / QA RA Manager / Quality and Regulatory Manager

Location: West Midlands, South Birmingham

Salary: £35,000 - £45,000 DOE potential to be flexible

I am currently working with a Medical Device Manufacturing Company who are seeking a Quality & Regulatory Manager to join their team on a permanent basis. This is a small company who are working on a range of developing products. It is not essential to have Regulatory experience. 

Experience which will be considered for this position are Precision Engineering or Medical Devices or a related industry. Man management/responsibilities is an essential requirement or the equivalent to leading a team.

The Quality & Regulatory Manager will be responsible for leading a small team made of QA focused and RA focused professionals. The role is either suited to someone who is looking to take the next step with their career or for someone who is seeking a fresh new challenge within a similar role now.

Personality and drive are both main factors for the right person and my client is seeking someone with a can-do attitude to join this team.


Role and Responsibilities to include:

  • Management of all the work related to the organization and functioning of the Quality System for compliance with current requirements of the Medical device Directive and ISO 13485/9001
  • Responsible for regulatory matters including Technical Files, Overseas registration, CE marking
  • Management of the Goods Inwards and Final Inspection areas
  • Ensuring that products meet the quality and performance requirements outlined in our quality system
  • Management and administration of Inspection Standards and Controls attributable to the Company’s Products, Raw Materials and Components
  • Monitoring inspection failures, supplier performance, production scrap, and Customer complaints; establishing methods for determining the root causes of failures; and identifying the solutions and costs required to remedy these causes, implementing and notifying the outcomes to management colleagues
  • Communicate and support the production personnel when there are changes to inspection standards
  • Maintain and update required records and documentation, including drawings and CAPAs.
  • Administration and Calibration of internal & external inspection equipment.
  • Allocation of tasks/projects so that each member of the team has clear objectives within clear defined timeframes
  • Preparation and communication of Quality KPIs. Liaison with corporate and external contacts with regards to quality issues
  • Other tasks as and when necessary
  • Cooperation with respective authorities in the scope resulting from binding regulations
  • Management and administration of the internal and suppliers auditing schedule
  • Labelling, Packaging, Regulatory processes, microbiology and Validations etc.
  • Responsible to conduct Management Review

Interviews can be arranged immediately, therefore, if you are interested, send your updated CV through to r.reichmuth@x4group.co.uk and call Renee on 0207 812 7700 to discuss in further detail.

Medical Devices / ISO 13485 / ISO 14971 / CE Marking / Technical File Review / FDA / CAPA / NCR / KPI / QMS

Apply for this job: Quality Manager - West Midlands

Contact Information:

Address:  Head Office
2nd Floor, Brettenham House
Lancaster Place,
London,
WC2E 7EN
England
Tel:  02078127700
Website:  Visit Our Web Site

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