Regulated Industry (Pharmaceutical / Medical Device)Great locationContract / Temp Opportunity We are currently seeking the services of an experienced Document Writer to join a busy medical device company.
With an emphasis on compliance and quality documentation, you will be a vital player in ensuring company adherence to a range of regulatory standards in product quality.
The fundamental requirement for this role is Standard Operating Procedure writing, and experience with evaluating and rewriting existing documents. The nature of this work is primarily documentation based, so you must be methodical, highly organized, and have excellent attention to detail.
Thus, with a focus on detail and an understanding of key regulatory requirements, you will have proven documentation skills from either a pharmaceutical or medical device environment.
Additionally, you will be a confident communicator with a demonstrated history of meeting timelines with accuracy.
This exciting role is well rewarded and conveniently located in the inner suburbs of Melbourne.
To submit your application in strict confidence, click the 'apply' button.
If you require further information, please contact Voula Triantafillou on 0437 853 201.
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