Senior Engineer/Specialist, Pharmaceutical Validation (Toronto) (Winnipeg)

Overview

Senior Pharmaceutical Validation Engineer or Specialist – Greater Toronto Area. The role involves managing validation activities, drafting master documents, executing qualification protocols, ensuring GMP compliance, supporting client QA teams, and managing client accounts. 5+ years of experience in pharmaceutical validation is required. Responsibilities

Draft master validation documents such as Validation Master Plan, risk analysis, cleaning matrix, and User Requirements Specification. Draft and execute equipment/system (IQ/OQ/PQ), process, and cleaning qualification protocols. Coordinate and ensure compliance with GMP during validation activities and general operations. Support clients’ QA/Compliance teams in initiating change notices or reporting deviations to trigger CAPA, Change Control, deviations, or other relevant actions. Manage client accounts. Requirements

Bachelor’s or master’s degree in science, engineering, or another relevant disciplin...