Quality Documentation Specialist

Job Overview

My client, a leading medical device manufacturing company are seeking a
Quality Documentation Specialist to join their team on a 12 month contract. There is an excellent salary package on offer for the right candidate.

Your new position:
As Quality Documentation Specialist, you'll be managing QMS implementation for the company manufacturing sites. This will include
- Updating Quality documentation
- Manage all documentation changes for MDR project
- Participate in project activities
- Change management activities for the implementation of MDR QMS requirements.

What You'll Need To Succeed:
- Previous experience of implementing documentation changes
- Working knowledge of change management systems/processes and documentation management
- Medical Device / cGMP or regulated industry experience

What you'll get in return:
You will be remunerated with an attractive salary along with bonus and generous holiday allowance You will be part of a focused team who work together and support one another with their workloads. The atmosphere is friendly and all employees are supported by peers and managers. Imagine working in a cutting edge world-class manufacturing environment where the demands are great but where there is ample opportunity to progress your career and advance your technical expertise with an employer that put a premium on talent development and employee engagement.

Your Next Step:
To apply for this position, please submit your CV through this website now in the strictest of confidence.

Have some questions? Call me for more information: Leo Cordingley 086 0495443

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