Ingénieur(e) Processus et Mécanique Pharmaceutique (GMP)

About the role

The company is seeking a Process and Mechanical Engineer to support pharmaceutical, biotechnological and life‑science manufacturing projects under GMP regulations. The role involves designing, analysing and optimising production processes while ensuring safety, performance and regulatory compliance.

Key responsibilities

• Design and optimisation of pharmaceutical and biotech manufacturing processes.
• Select, integrate, improve and provide technical support for production equipment, mechanical systems and clean utilities.
• Prepare and review engineering documents such as URS, P&ID, process flow diagrams, mass balances, technical specifications and equipment lists.
• Participate in GMP engineering projects, upgrades, expansions or new facility installations, coordinating with internal teams, clients and suppliers.
• Identify technical issues, perform root‑cause analysis, propose practical solutions and drive continuous improvement.

Required profile

• Permanent, unrestricted work authorization in Canada.
• 2–5 years of professional experience in pharmaceutical or biotechnological process and mechanical engineering.
• Strong knowledge of GMP environments and related regulatory standards.
• Proficiency in French language.

Required skills

• Process engineering for pharmaceutical/biotechnological production.
• Mechanical engineering applied to production equipment.
• Knowledge of GMP requirements.
• Ability to read and prepare URS, P&ID, specifications, process schematics and equipment lists.
• Proficiency with AutoCAD or equivalent CAD software.
• Proficiency with MS Project or equivalent scheduling tools, including Gantt chart creation.