What we offer:
On our books we have a comprehensive list of capable, professional staff accustomed to working to the TGA, FDA and Medsafe requirements:
Chemists experienced in Laboratory Instrumentation, LIMS, and Method Validation to the FDA and TGA regulatory requirements.
Technical Document Writers, with Pharmaceutical, Biotechnology and Medical Device industry experience, skilled in writing validation documentation and standard operating procedures.
Engineers, experienced in the pharmaceutical and medical device environment in various engineering disciplines to perform your validation cost-effectively.
Process Validation Technicians experienced in process validation.
We have a "can do" attitude and are always looking for variety and challenges beyond the daily grind. So, if you have a tough problem, we are confident we can supply the right person at short notice. No assignment is too short or too complex.
And all this at very affordable rates.
How it works:
You simply phone or email us with your requirements and we will respond with suitable staff within days.
Head quartered in Melbourne, Australia, we operate throughout Australia, New Zealand, South Africa and South East Asia.

