Manage validation activities for pharmaceutical systems, ensuring compliance through design, execution, and documentation of CQV protocols. Collaborate within teams to assess risks and maintain records for quality assurance in dynamic environments.

Tackle complex CQV tasks by designing validation plans, documenting assessments, executing engineering studies, and ensuring compliance through meticulous record-keeping in a fast-paced, collaborative environment, with strong focus on the pharmaceutical sector.

Unlock potential by overseeing Quality Assurance for GMP manufacturing, ensuring compliance for Cell & Gene Therapy products. Collaborate cross-functionally to drive quality initiatives and mitigate risks throughout the product lifecycle.