Job Description
LAPORTE is a consulting engineering firm specializing in pharmaceutical, agrifood, industrial biotech, and industrial plant processes. With 25 offices across North America and Europe and over 480 employees, the company has a 25‑year history of engineering excellence. This role is based in Burnaby, BC, and is part of the Greater Vancouver team. Responsibilities
Drafting master validation documents (e.g., Validation Master Plan (VMP), risk analysis, cleaning matrix, User Requirements Specification (URS)). 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 within the scope of validation activities. Manage client accounts. Requirements
Bachelor’s or master’s degree in science, e...
Drafting master validation documents (e.g., Validation Master Plan (VMP), risk analysis, cleaning matrix, User Requirements Specification (URS)). 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 within the scope of validation activities. Manage client accounts. Requirements
Bachelor’s or master’s degree in science, e...