Quality Manager - new job in Blackburn, UK

Quality Manager
  • Competitive
  • Permanent
  • Blackburn, Lancashire, England, UK Blackburn Lancashire UK BB1 2QJ
Job Ref: J2166393
Sector: Engineering
Sub-sectors: Biotech/Life Sciences, Pharmaceuticals, Medical Devices
Date Added: 01 September 2022
Are you an experienced Quality Manager looking for a fulfilling role with a lot of responsibility? Please apply below!

Quality Manager - LancashireSRG are currently recruiting for a quality manager to join a medical device consultancy based in the Lancashire area This will be on a permanent basis, at a competitive salary.The quality manager will be developing and managing the company's quality management system in compliance with the requirements of ISO 13485. You will be developing the company-wide processes to facilitate the continued growth within the global market. You will also be the company's gatekeeper for the release for sale of products to ensure that the devices meet all quality and safety requirements before release to the customer.Day to day activities include but are not limited to:* Strategic planning, management, and implementation of the QMS and its sub-systems and processes and ensuring that its development meets business and regulatory needs. * Managing members of your Quality team, their output and ensuring their continued training & development. * Ensure that audit capability is developed and maintained as required by business needs and perform internal and external audits as required by the relevant schedules/subject matter expert and take the lead in hosting customer audits* Ensure that the complaints and non-conformance systems, and CAPA, are managed effectively and to timely conclusion.* Use the analysis of information received through customer complaints, non-conformance reports, audit reports, CAPA and other relevant quality data, to make conclusions and drive actions for improvements and compliance.* Deliver and plan/propose training in QMS topics to all levels of the business and support all staff inductions.* Adhere to QMS, HSE policies and procedures and all other Mi3 policies and procedures at all times.Qualifications, experience and person specification:* Bachelor level degree or equivalent in a relevant Quality Management, Engineering or Science discipline.* Minimum of 5 years' experience within a manufacturing based medical devices business regulated to ISO 13485 in a quality role, with good, all-round knowledge of medical device quality systems.* A minimum of 5 years' experience in a high-level position with demonstrable successes in leading and inspiring teams.* Demonstrable experience in quality engineering field / topics such as process control, error proofing, failure investigation and root cause analysis, CAPA, data collection and analysis, batch records, in-process testing/checks, CTQs, defect classifications, visual standards, GR&R, change management, and the application of statistics.* Familiar with Gamma and EO sterilisation processes and microbiological requirements for medical devices.* Successful with influencing and driving results.To find out more information, please apply or email Jessica.oconnor@srgtalent.com

SRGTalent https://www.srgtalent.com https://www.srgtalent.com/-/media/srg/1---new-website/logos/website-logo-all-padding-removed.png
01/10/2022 16:28:39
GBP 50000 55000 Annum
Contact Consultant:
Jessica O'Connor

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