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May 21 2018

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Offer: Quality Systems Manager:Real Life Sciences

Job description:

Quality Systems Manager

Real Life Sciences

   » Waterford
   » See description
   » Permanent full-time
   » Updated 16/05/2018
   » Roisin Finneran this job is expired SaveSave Apply Now

Job detail

A leading medical device manufacturer in Waterford are looking for a Quality Systems Manager. If you're an expert in this area and seeing a new challenge, then this could be the function for you.

Why should I apply for Quality Systems Manager?
My client are a medical device organisation located in Waterford. They require a Quality Systems Manager on a permanent basis to join them. You will be working in one of the world's most recognised manufacturers of their medical device product. As their operations have expanded in Waterford, it's an excellent time to join them during their growth period.
You will be involved in the set-up, maintain and improve the legal manufacturers QMS and to participate in the delivery of QMS changes for MDR implementation.
You will also participate in the implementation of MDR for all the medical device sites which includes performing gap assessment for MDD, ISO and MDR identifying and remediating gaps in the QMS and change management activities for the implementation of MDR QMS requirements
What will be main responsibilities be?
   » Setup, maintenance and continuous improvement of Quality Management System the medical device legal manufacturer
   » Responsible for updating the QMS for the legal manufacturer & business unit QMS to comply with existing & emerging quality regulations & standards
   » Responsible for working with functions, outsourced processes & manufacturing to determine the legal manufacturer architecture, connected documentation and connected governance
   » Lead the legal manufacturer audits with significant authorities & internal compliance group
   » MDR project activities as outlined by Manager
What do I need to apply for Quality Systems Manager?
   » Bachelor's Degree in a quality, scientific or engineering discipline
   » Minimum of 5 years related work practice in the Medical Device industry
   » Thorough expertise of Quality Systems, Quality Assurance, and regulatory requirements.
   » Excellent report writing and documentation expertise.
   » Specific expertise of legal manufacturer requirements as defined by EU legislation is necessary.
   » Broad regulatory and standards expertise in the medical device sector
   » EU Passport/Stamp 4 Visa needed for consideration.
Interested in this opportunity in Waterford? Want to hear more? Apply now and I can follow up with you.

To find out more about Real please visit
Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales
Ref: RE-32879258_1525175311
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Real Life Sciences


   » 3rd Floor, 80 Harcourt Street, Dublin 2
   » 01 8883477


Job Category: Customer Service [ View All Customer Service Jobs ]
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Employment type:
Salary: Unspecified
Degree: Unspecified
Experience (year): Unspecified
Job Location: Waterford
Company Type Employer
Post Date: 05/16/2018 / Viewed 10 times
Contact Information
Company: Real Life Sciences

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