Process Validation Engineer

we are in the pharmaceutical industry and looking for Process Validation support for manufacturing of fill/finish products. Day-to-Day Responsibilities we are looking for a process validation engineer who can generate process validation protocols, summary reports and understand what documentation is required from CQV through the process validation lifecycle. You should have a great understanding of what critical process parameters are vs. non-critical process parameters. It is required to be able to support PV readiness, complete risk assessments and own Process Validations from end to end. You will be providing the oversight of batch executions/manufacturing from a process validation perspective in order to be able to raise concerns throughout the process and correct as needed. Job Types: Contract, Full-time Pay: $50.00 per hour Schedule: 8 hour shift Day shift Education: Bachelor's (Required) Experience: process validation: 2 years (Required) CQV: 2 years (Required) Validation protocols: 1 year (Required) Critical process parameter: 1 year (Required) PV readiness: 1 year (Required) Work Location: In person