We are seeking a Validation Engineer to support EO sterilization validation activities within a regulated manufacturing environment. This role will focus on supervising and coordinating Performance Qualification (PQ) execution activities while ensuring compliance with GMP and ALCOA documentation standards.
The ideal candidate will have hands-on experience with sterilization validation processes strong coordination skills and the ability to support cross-functional execution activities in a fast-paced environment.
Key Responsibilities
Supervise execution of EO sterilization Performance Qualification (PQ) activities
Coordinate half-cycle nominal/full-cycle and maximum-cycle sterilization runs
Prepare and manage PCDs (Process Challenge Devices) and Biological Indicators (BIs) for shipment and cycle insertion
Support preparation and arrangement of dunnage for EO sterilization processes
Oversee movement of product loads through refrigerated storage tempering sterilization and aeration processes
Coordinate retrieval and shipment of PCDs BIs and product samples for Quality Control testing
Ensure execution activities and documentation comply with ALCOA principles and GMP requirements
Collaborate with Validation Quality and Operations teams to support project timelines and execution
Required Qualifications
Experience in validation within medical device pharmaceutical or regulated manufacturing environments
Hands-on knowledge of EO sterilization validation and PQ execution activities
Strong understanding of GMP documentation practices and ALCOA principles
Ability to coordinate cross-functional activities and manage execution timelines
Strong communication and organizational skills
Job Title: Validation Engineer Location: Fort Worth TX (Local candidates only) Travel: Required Alabama (3 4 weeks expenses paid) Duration: 3 6 Month Contract Start Date: Immediate Job Summary We are seeking a Validation Engineer to support EO sterilization validation activities within a ...
We are seeking a Validation Engineer to support EO sterilization validation activities within a regulated manufacturing environment. This role will focus on supervising and coordinating Performance Qualification (PQ) execution activities while ensuring compliance with GMP and ALCOA documentation standards.
The ideal candidate will have hands-on experience with sterilization validation processes strong coordination skills and the ability to support cross-functional execution activities in a fast-paced environment.
Key Responsibilities
Supervise execution of EO sterilization Performance Qualification (PQ) activities
Coordinate half-cycle nominal/full-cycle and maximum-cycle sterilization runs
Prepare and manage PCDs (Process Challenge Devices) and Biological Indicators (BIs) for shipment and cycle insertion
Support preparation and arrangement of dunnage for EO sterilization processes
Oversee movement of product loads through refrigerated storage tempering sterilization and aeration processes
Coordinate retrieval and shipment of PCDs BIs and product samples for Quality Control testing
Ensure execution activities and documentation comply with ALCOA principles and GMP requirements
Collaborate with Validation Quality and Operations teams to support project timelines and execution
Required Qualifications
Experience in validation within medical device pharmaceutical or regulated manufacturing environments
Hands-on knowledge of EO sterilization validation and PQ execution activities
Strong understanding of GMP documentation practices and ALCOA principles
Ability to coordinate cross-functional activities and manage execution timelines