Pharma Validation Engineer - Revalidation & GMP Compliance

United Pharma Technologies Inc

North Carolina

On-site

USD 85,000 - 115,000

Full time

2 days ago

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Job summary

United Pharma Technologies Inc is seeking Validation Engineers to support annual revalidation activities for fill-finish manufacturing operations at a pharmaceutical site in Greenville. The role involves executing and reviewing validation protocols (IQ/OQ/PQ), along with supporting sterilization revalidations and associated documentation, while ensuring GMP and FDA compliance.

Collaborate with Manufacturing, Engineering, QA, and Validation teams to review records and maintain deviation/change

Qualifications

Hands-on experience with pharmaceutical/biotech validation.
Strong background in fill-finish, filling, and/or sterilization validation.
Experience supporting annual revalidation programs in a GMP environment.
Familiarity with validation documentation, deviations, and change controls.

Responsibilities

Support annual revalidation activities for fill-finish and filling processes.
Execute and review validation protocols, including IQ/OQ/PQ and process revalidation.
Support sterilization revalidation activities and associated documentation.
Review equipment, process, and cleaning validation records for compliance.
Work closely with Manufacturing, Engineering, QA, and Validation teams.
Ensure validation activities comply with GMP, FDA, and site procedures.
Prepare and maintain validation reports, protocols, deviations, and supporting documentation.