VALIDATION SPECIALIST

Employer
AUMVIS PHARMATEC LLC
Location
McLean, Virginia
Posted
Sep 10, 2017
Closes
Sep 24, 2017
Function
Other
Industry
Other
Hours
Full Time

Validation Specialist (Mclean, VA). Write & execute IQ (Installation Qualification), OQ (Operational Qualification) & PQ (Performance Qualification) validation protocols & reports, initiate deviations, & determine root cause & prescribe corrective & preventative actions. Perform dvlpmt & validation studies for Clean in Place (CIP) & Sterilize in Place (SIP), Author pharmaceutical dvlpmt techn'l reports & rltd Common Technical Document (CTD) sections & serve as expert scientific resource for regulatory filings. Master's deg in field of Bio Chem., Chem., Pharmacy or rltd field w/ 2 yrs work exp OR employer will ultimately accept Ph.D deg in field of Bio Chem., Chem., Pharmacy or rltd field. Work exp must incl exp w/ pharmaceutical dvlpmt setting w/ dsgn & execution of experiments incl implmtn of DOE & QbD principles. Must have executed, dvlpd & qualified a variety of mfg processes. Resumes: Aumvis Pharmatec LLC, 2010 Corporate Ridge Dr, Ste 715, Mclean, VA 22102

Similar jobs

More searches like this