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Franklin Bio Lab
In Vivo Training and Validation Specialist
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What they do
A Validation Specialist tests and documents the validity and accuracy of manufacturing systems and equipment. Tests processes and manages process validations. Provides technical support and implements operating procedures. May create documentation to show that a manufacturing or production process has consistent results and meets quality standards.
$85,090 / year median in Pennsylvania
+4% projected growth
Job Description
Franklin Biolabs emerges from the esteemed legacy of Dr. Jim Wilson's laboratory, a beacon of innovation in vector technology for over three decades. Building on this rich heritage, Franklin Biolabs is poised to redefine the landscape of the global genetic medicines industry. As a Contract Research Organization (CRO), Franklin Biolabs offers a comprehensive suite of services spanning from discovery through clinical manufacturing. Our goal is to empower our partners by providing unparalleled solutions that drive the advancement of genetic medicines. Leveraging decades of expertise and a commitment to excellence, we bridge the gap between groundbreaking research and ensuring that transformative therapies reach those who need them most. The In Vivo Training & Validation Support Specialist is responsible for developing, delivering, and documenting technical training programs for research personnel, while concurrently providing hands-on technical support for laboratory equipment qualification as needed. This role ensures vivarium staff are proficient in animal bio methodologies and that all critical equipment used in animal research is verified and maintained in compliance with institutional guidelines (e.g., GLP, IACUC, AAALAC). Reporting to the In Vivo Training Coordinator, this position works closely with technical staff, trainers, study teams, veterinary staff, and quality personnel to ensure staff proficiency, accurate training records, and compliance with company procedures and regulatory expectations. This role serves as a key resource for training logistics, qualification tracking, procedural observations, and documentation management to support a skilled and compliant workforce. While this role executes equipment validation testing and drafts protocols for animal research-related activities, final regulatory accountability and sign-off rest with Study Directors and Test Facility Management.