QMS Manager

I’m currently looking for a QMS Manager to join a Diagnostics and Medical Device business company based in the Essex region. As the QMS Manager, you will be responsible for multiple Quality Management systems, as well as the following:

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the QMS Manager will be varied, however the key duties and responsibilities are as follows:

1. Implement and develop all aspects of the Quality Management Systems, ensuring they comply for the following; ISO 17025:2017. ISO 14001:2015, ISO 13485:2016, and ISO 27001:2013.

2. Prepare technical documentation for new products to submit to Regulatory Bodies as required.

3. Develop an audit schedule for the business as well as carry out internal audits and subsequent audit reports.

4. Monitor the complaint processing system to ensure effective and timely resolution, as well as participating in investigations of customer complaints.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the QMS Manager we are looking to identify the following on your profile and past history:

1. Relevant and demonstrable experience of ISO 17025:2005/2017 and ISO 13485:2016

2. Proven industry experience within a Laboratory or Medical Device manufacturing environment

3. A working knowledge and practical experience of Quality Management Systems


Key Words: QMS, Quality Management, Systems, 17025, 13485, Quality, Diagnostics, Medical Device

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.