Job Title : Senior Validation Engineer – Visual Inspection Systems
Location : Remote
Client : Regeneron Pharmaceuticals
Overview :
Seeking an experienced Validation Engineer to support visual inspection system qualification and requalification activities within Regeneron’s fill-finish operations. The role involves developing and executing validation deliverables for semi-automatic and fully automatic inspection equipment and ensuring alignment with cGMP and corporate standards. This position requires a high degree of technical expertise to complement a team of mid-level validation contractors.
Key Responsibilities :
- Developed, reviewed, and executed validation protocols (IQ / OQ / PQ) and requalification programs for visual inspection systems in sterile manufacturing.
- Supported SAT and commissioning activities for semi-automatic syringe inspection (SASI), semi-automatic vial inspection (SAVI), and SWITCH systems .
- Created equipment-specific validation documentation from the ground up, ensuring templates and protocols accurately reflected fill-finish processes rather than bulk manufacturing setups.
- Evaluated and optimized inspection system performance through Knapp studies, ensuring consistent visual inspection accuracy and reliability.
- Authored technical reports, risk assessments, and validation summaries in compliance with FDA, EU Annex 1, and internal quality standards.
- Collaborated with automation, quality, and manufacturing teams to troubleshoot equipment performance issues and drive continuous improvement in inspection reliability.
- Established and maintained a requalification strategy for automated inspection systems, incorporating data-driven lifecycle management principles.
- Provided mentorship and technical guidance to junior validation engineers and contractors.