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Quality Manager

Surrey   •  £54,000 - 56,000  •  Permanent, Full time


Quality Manager

Permanent position

5 days a week- on site Guildford based

56,000 annual salary, 25% annual bonus and annual company stock shares

An exciting opportunity to join a pharmaceutical company specialising innovative medical devices in sexual and pain health as a quality coordinator. The Quality Manager will report to the Head of Quality and performance of operational quality processes.

Job responsibilities include:

Overseeing the day to day and being responsible for running the MD QMS

Be adhering and compliant with FMDs, SOPs and MD SOPs

To be designee to the Regulatory Affairs Director when acting as the person responsible for (PRRC)

Ensure procedures and systems are maintained or established to maintain the Companys compliance with ICH Good Clinical Practice; current national and international legislation; and relevant regulations, standards and guidelines

Responsible for ensuring distribution and documentation of receipt of procedures amongst staff within the company and the virtual team

Directing and maintaining training programmes for employees

Follow procedures and systems to maintain company compliance with ISO 13485 and enable the manufacture of medical devices in accordance with governance national and international legislations, standards, guidelines and relevant regulations

Comply with the companys compliance ICH Good clinical practice

Liaise with third party organisations and health authorities to resolve quality related issues and represent the company

Responsible for evaluating and reviewing third party quality incident reports

Oversee and manage business operating procedures

Management of a small team

Candidate essential skills and requirements:

Graduate

5+ years professional experience in Regulatory Affairs or Quality Management systems relating to medical devices

Good knowledge and experience with quality management systems e.g. ISO 13485, GCP, GMP, GDP, EU regulations 2017/745 on Medical Devices (MDR)

Successful MHRA/Notified bodies

Significant professional experience in quality management relating to pharmaceuticals

Project management skills and ability to manage a team

To apply contact: hanan.gibson@cpl.com | 0118 952 2798

  • Agency: Cpl Life Sciences
  • Contact: Hanan Gibson
  • Reference: JO-2110-477649
  • Posted: 5th October 2021
  • Expires: 2nd November 2021

Cpl Life Sciences

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