* Execute validation and verification test procedures consistent with established FDA and ISO regulatory requirements. * Performed and wrote tests and reports for Phase 1 and Phase 2 system integration testing for the phacoemulsification surgical system.* Performed ad-hoc testing on all new and interim software builds for software developers to discover “bugs” prior to releasing the software builds for validation.* Actively involved in formal verification and validation activities of next-generation medical devices following GDP per corporate SOP standards that are in compliance with FDA requirements.* Updated specifications, generated test protocols, and completed validation for On-line Calculator software for planning the implantation of intraocular lenses.* Generated test protocols to complete validation for Human Factors Engineering and Risk Assessment for Phacoemulsification Surgical System.* Authored validation and verification test procedures that are consistent with established FDA and ISO regulatory requirements.* Red-lined and updated software user manual for phacoemulsification surgical devices.* Write Software Test Procedures consistent with established FDA and ISO regulatory requirements. * Write Software Requirements Specifications consistent with established FDA and ISO regulatory requirements. * Practice SCRUM and Agile methodologies and participate in daily stand-ups.

* Execute validation and verification test procedures consistent with established FDA and ISO regulatory requirements. * Write Software Test Procedures consistent with established FDA and ISO regulatory requirements. * Write Software Requirements Specifications consistent with established FDA and ISO regulatory requirements. * Write, review, and maintain the Traceability Matrix.* Testing the pack using cataract surgery like OPO 73 & OPO 71.* A brief summary of the project description below: Several J&J cataract surgery systems including Sovereign Compact, Signature WhiteStar, and Compact Intuitiv (Apollo)