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.