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Specialist-Validation/ Manufacturing/Pharma / Bio / Medical Device
Randstad Engineering
Randstad Engineering
 
Job Location: THOUSAND OAKS, CA
Large pharmaceutical manufacturer has an immediate need in Thousand Oaks CA for Validation Specialist to plan, schedule, execute and lead validations for manufacturing processes including participating in the design/development stage and leading the validation phase for manufacturing processes. This is a contract opportunity expected to last 1 year could be longer based on performance, possible temp to perm. Apply Now

Responsibilities:

-> Provides technical and project leadership over validation in support of company projects, support of manufacturing operations
-> Ensure validation master plans comply with regulatory agency requirements
-> Support development of best demonstrated validation practices within the validation department, based on current industry practices and guidelines
-> Schedule, plan and manage qualifications of systems including manufacturing processes, equipment and materials to ensure adherence to specifications
-> Analyze large amounts process data using various statistical tools to determine the acceptability and performance of equipment, materials, processes and products

Requirements:

-> Minimum of BA or BS in Chemistry, Biotechnology, Biochemistry
-> 10+ years related experience or 4+ years related experience w/ an advanced degree or demonstrated performance within a GMP regulated environment within the pharmaceutical industry
-> Knowledge of GMP/manufacturing environment and regulatory compliance for the manufacturing of bulk and finished products


Related Words: validation engineer, bio, pharma, medical device, manufacturing




Randstad Engineering

 
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