Integrator, operational optimisation

MAIN RESPONSIBILITIES

• Constantly optimize the performance and efficiency of our processes in line with the growth of production volumes;
• Review the organization of workstations, assembly methods, and production sequences;
• Conduct economic cost reduction analyses to select the best opportunities;
• Play a pivotal role and be the link between cost reduction projects and production reality;
• Establish methods for maximum utilization of production facilities and personnel;
• Facilitate continuous improvement activities in the form of Kaizen;
• Recommend changes and organize their implementation;
• Produce production reports;
• Conduct time and motion studies to bring about the best process improvements;
• Map production processes to eliminate bottlenecks and optimize production output;
• Facilitate the implementation of performance indicators;
• Take charge of the production transfer for large-scale manufacturing of new products;
• Implement processes and procedures respecting the quality system;
• Plan and participate in equipment and process validation activities (IQ, OQ, PQ).

POSITION REQUIREMENTS

• Diploma in Industrial Engineering, Automated Production Engineering, or Operations and Logistics Engineering; - Minimum of 7 years of relevant experience as an industrial engineer in the manufacturing sector;
• Experience in project management and technical writing;
• You have good methods for complex problem solving;
• You demonstrate strong leadership skills and a high sense of initiative;
• You stand out for the quality of your communication, promoting teamwork;
• You have a keen sense of analysis and synthesis;
• You possess a strategic vision for projects;
• You are customer-focused;
• Very good command of the French language and good knowledge of the English language (oral and written);
• Member of the Ordre des Ingénieurs du Québec.

ASSETS

• Experience in the medical field;
• Experience in robotics or with mechatronic systems;
• Knowledge of SolidWorks, JIRA, and Confluence;
• Experience with repeatability and reproducibility tests (Gage R&R) and statistical methods;
• Knowledge of quality management principles and methodologies (ISO 13485);
• Knowledge of FDA quality system regulations (21 CFR Part 820);
• Experience with one or more of the following standards: IEC 60601, IEC 60204,ISO 13849, and UL1740.1.

WHAT WE OFFER

• Remote work (according to job type);
• Competitive salaries;
• Group RRSP with employer contribution;
• Group insurance paid at 50% by Kinova;
• Up to 4 weeks of vacation;
• Personal days off in addition to vacation;
• Snacks, coffee, and fresh fruit at all times;
• A dedicated and great work team;
• A state-of-the-art environment;
• A company culture focused on the development of each individual;
• Free parking;
• Electric vehicle charging stations;
• Regular social and sporting events;
• And much more, but you'll have to meet us to learn more…