Job Description
LAPORTE is seeking a senior pharmaceutical validation engineer or specialist with ideally at least 5 years of experience in the validation and qualification of pharmaceutical equipment to join its Greater Calgary team. Our validation engineer will play a key role in managing validation activities, including drafting master documents, executing protocols, and ensuring compliance with Good Manufacturing Practices (GMP).
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 our clients’ QA/Compliance teams in initiating change notices or reporting deviations to trigger CAPA, Change Control, deviations, or other relevant actions within the scope...
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 our clients’ QA/Compliance teams in initiating change notices or reporting deviations to trigger CAPA, Change Control, deviations, or other relevant actions within the scope...
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