VALIDATION SPECIALIST

Expiring today

Employer
AUMVIS PHARMATEC LLC
Location
McLean, Virginia
Posted
Sep 10, 2017
Closes
Sep 23, 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

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