Overview
Full Time
Part Time
Accepts corp to corp applications
Contract - Independent
Contract - W2
Skills
Profit And Loss
GxP
IQ
OQ
PQ
URS
FRS
SDS
Risk Assessment
Change Control
Auditing
Communication
Project Coordination
Pharmaceutics
Regulatory Compliance
Job Details
Title: Validation specilist
Location : San Diego CA
The client is seeking a Validation Specialist with strong expertise in GxP-regulated environments, particularly in documenting and executing validation protocols (IQ/OQ/PQ) for equipment, software, and processes. They need someone experienced in authoring and reviewing full validation lifecycle documents (URS, FRS, SDS, etc.). The role involves risk assessment, change control, audits, and start-up support for facility and process equipment. Strong communication and project coordination skills across multi-disciplinary teams are essential. Familiarity with biotech/pharma environments, especially fractionation processes and compliance, is highly preferred.
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