QA Systems and Validation Specialist
Westbourne IT Global ServicesJob Description
Position Summary
The QA Systems & Validation Specialist is responsible for ensuring that all GMP-related changes, systems, and validation activities comply with regulatory requirements and site Quality standards.
This role provides subject matter expertise across change control, validation, and quality systems, supporting manufacturing, laboratory, engineering, and IT operations within a regulated pharmaceutical environment.
Key Responsibilities
Quality Systems & Change Control
Assess GMP impact of changes in accordance with site Change Control procedures for:
Facilities and utilities
Laboratory and manufacturing equipment
Control and automation systems
Ensure changes are appropriately evaluated, documented, and approved for GMP compliance.
Validation & Compliance
Provide validation expertise to ensure compliance with c...
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