The Company
You will be working for an ASX-listed global manufacturer that has been in operation for the last 20 years, with offices across Australia, the USA, Canada, the UK and Europe. With a global HQ and manufacturing site in Sydney, they are developing and manufacturing an Australian-made product used across the globe.
The RoleIn this role you will be supporting a project team with updating the QMS documentation, this will require you to be organised, detailed orientated and proactive. You will ensure that the documentation is written, edited using the standards and policies in place. This position will require you to have experience with QMS in the medical device industry.
This position is a short term, casual position to support a project team that is introducing a new product. The organisation standard operating hours are Monday-Friday.
About You
- Previous experience as a Technical Writer
- Background in the medical device industry
- Experience with Quality Management Systems
- Experience in producing technical and business process documentation
- Experience producing manufacturing documentation
- Strong understanding of document styles and templates
- A high level of attention to detail
- Excellent communication skills
- Be able to work at part of a project team
Contact Details
We are recruiting and interviewing candidates immediately for this role so if you meet the above criteria and would like to be considered for this role for an ASAP start, please click 'APPLY' now.
Alternatively, you can contact Christine (Division Manager) at KE Select on 0478 144 103 / christine@keselect for a confidential discussion.
KE Select are a leading provider of Scientific, Medical and Technical recruitment services. With a candidate and client network spanning ANZ and more recently into APAC, KE Select are no.1 choice for many professionals operating within the Biotechnology and Medical Technology market.
