BioTeknica Inc. is a leading consulting firm specializing in engineering, quality and
regulatory projects for the medical device, pharmaceutical and biotechnology industries. Our
clients include major manufacturers within these industries worldwide.

 

We are currently have opportunities in the Southeast and Midwest for contract engineers with
Validation experience in the Medical Device industry.

 The successful candidate will have a B.S. in Engineering or Life Sciences;

3 � 5 years of hands-on validation experience within the medical device industry (developing,
executing and writing final reports for IQ, OQ, PQ  protocols). 

All potential candidates must have: statistics experience; a good understanding of the
guidelines governing regulated manufacturing operations (ISO, cGMP, QSR, state and local
regulations).  Must have strong written and verbal communications skills and be computer
literate with Word, Excel, Visio, MiniTab or similar software applications.  Must be able
travel extensively.