Job Title: Equipment Validation Engineer
Summary:
Responsible for the planning, execution, and documentation of equipment qualification and validation activities within a GMP-regulated pharmaceutical manufacturing environment.
Responsibilities:
* Develop and execute validation protocols (IQ, OQ, PQ).
* Generate and maintain accurate validation documentation.
* Perform risk assessments related to equipment validation.
* Coordinate with cross-functional teams (QA, manufacturing, engineering).
* Ensure compliance with GMP and relevant regulatory guidelines.
* Troubleshoot and resolve validation deviations.
* Manage equipment calibration and maintenance related to validation.
* Review and approve validation related documentation.
Qualifications:
* Bachelor's degree in Engineering or a related science field.
* Experience in equipment qualification and validation in a GMP environment.
* Strong understanding of GMP regulations and industry standards.
* Excellent documentation and communication skills.