Description
LAPORTE is hiring a senior pharmaceutical validation engineer or specialist for its Greater Montreal team. The role manages pharmaceutical equipment and system validation and qualification, including master documents, IQ/OQ/PQ, process, and cleaning protocols; coordinates GMP compliance; supports quality-assurance activities such as change notices, deviations, and CAPAs; and manages client accounts. Candidates need a bachelor's or master's degree in science, engineering, or a relevant discipline, pharmaceutical or consulting experience, GMP knowledge, knowledge of pharmaceutical manufacturing processes, and willingness to travel to client sites. The position offers medical, dental, and vision coverage, vacation, retirement contributions, and other benefits.
