Company: Our client is a leading US Pharmaceutical company with operations in over 30 countries worldwide. They have their European Shared Service Centre in Ireland and are supporting their internal and external customers from this central operation. Their European Support Centre is based in Dublin.
Role: They are currently looking for reliable and experienced quality assurance specialist. In this role your main task will be the examination and confirmation of the document modification requests. You will authorise the issue of new documentation according with the company quality guidelines and operating procedures. You will also support and participate in the elaboration of an effective complaints handling system.
Skills: To apply for this role you will need to have 2-3 years experience in the sector of medical and or pharmaceutical apparatus. You will have an in depth knowledge of the Medical Devices Directives, the ISO standards related with medical devices and risk management. The profile that we are looking for this role is the one of a proficient technical writer with ability to multi-task and optimal organisation and analytical skills.
Gain: This is a great opportunity to join an internationally oriented team based in Ireland. This role is a great opportunity for graduates in biology, pharmacology, chemistry and life science who are keen to start a great career in the high potential quality control sector. So if you are up for the challenge contact the recruitment team in BeesWax Europe and take your career to the next level.
Ireland: +353 1 685 4448
Germany: +49 69 5007 1333
Netherlands: +31 202 015 444
DX1895
info@beeswaxeurope.com
No comments:
Post a Comment