Senior Validation Engineer

40 hours/ week.

Skills:

Participate in contracted validation projects within the pharmaceutical and biotech industries, including managing, leading, preparing, reviewing and execution of validation protocols (IQ/QQ/PQ) and Process Validation Master Plans
Generation of final reports for commissioning, qualification and validation
Test to verify any installed parts and components to ensure system are functioning per client design, specifications and operating requirements
Qualify systems for installation, operation and performance through systematic examination and execution of protocols; validate/ verify that the systems and processes are capable of producing the results specified in predetermined criteria under specified conditions; utilized systems include manufacturing tanks, tablet presses, coating machines, lyophilizers, COP washers, process vessels (such as buffer and precipitate vessels), CIP skids, filter presses, centrifuges and chromatography skids (nano and UF-DF).
Experience:

Qualified applicants will have a Masters degree in Pharmaceutical Manufacturing/ Engineering plus 12 months of experience in Cleaning Validation Engineering. Position Location: Brockton, Massachusetts. Please send a resume and cover letter to VTI, Mr. Ed Winnett, VTI, 912 Crescent Street, Suite 2; Brockton, MA 02302.
Posted 4/21/2017 2:20pm p.s.t.