Senior Project Manager

Job Summary Reporting to the EVP Global Strategy & Technical Operations, the Senior Project Manager is accountable for execution and support of high value, complex & strategic capital projects across the Bimeda North America manufacturing site network. The manufacturing site network currently incorporates Bimeda MTC, Cambridge, Ontario, Bimeda Le Sueur, Minnesota and Bimeda Biologics, San Angelo, Texas. The Senior Project Manager will lead Bimeda’s strategic capital projects through their entire lifecycle, overseeing scope, budget, timelines, risk, and stakeholder communication, from initial planning to post‑completion evaluation. Key responsibilities include developing the project charter and management plans, collaborating with cross‑functional teams to define and manage project elements, ensuring quality and risk mitigation, managing budgets, and acting as the primary interface between the project and its stakeholders to achieve objectives. Prepare detailed capital project justification submissions for large‑scale, multi‑disciplinary projects, ensuring alignment with strategic business objectives. Demonstrates an expert level of operational knowledge of pharmaceutical and/or biological manufacturing processes, systems and equipment. Demonstrates a thorough understanding of good manufacturing practices (GMP), good documentation practices (GDP), regulatory guidance requirements, safety and environmental controls. The Senior Project Manager will have experience operating within a PMO environment, using Project Management Software (PMS) applications to manage a portfolio of projects. Role Specific Requirements Lead the end‑to‑end delivery of capital projects, including scope definition, planning, execution, monitoring, and closure. Develop and manage project budgets, forecasts, and cost control systems, ensuring projects are delivered within approved financial parameters. Build and manage detailed project schedules, ensuring the timely allocation of resources across engineering, construction, and validation teams. Identify, assess, and mitigate project risks; implement robust contingency and change management processes. Ensure all projects are executed in strict compliance with cGMP, FDA, Health Canada, and other relevant regulatory and safety standards. Act as the primary liaison for senior leadership, site management, and external partners; provide regular updates and transparent reporting on project performance. Lead the selection, negotiation, and management of engineering firms, contractors, and suppliers to ensure performance and accountability. Oversee project handover, commissioning, qualification, and validation processes to ensure seamless integration into operations. Promote best practices, standardization, and lessons learned across the capital project portfolio to drive ongoing improvement in project execution. Technical & Functional Expertise Strong knowledge of cGMP, FDA, Health Canada, and ICH guidelines as they relate to pharmaceutical manufacturing and facilities. Expertise in engineering design, construction management, commissioning, and validation of pharmaceutical facilities, utilities, and equipment. Proficiency in project management methodologies (PMP or equivalent certification preferred). Experienced in using Project Management Software for discrete project management and also as a PMO portfolio reporting tool. Experience with project controls (cost estimation, scheduling, risk management, and change management). Leadership & Communication Ability to lead and influence cross‑functional teams and external contractors in a matrixed environment. Exceptional stakeholder management skills, with the ability to communicate effectively at all organizational levels, including executive leadership. Demonstrated success in negotiating vendor contracts and managing third‑party engineering and construction firms. Operational & Strategic Skills Proven ability to balance strategic planning with hands‑on execution in highly regulated environments. Strong analytical, problem‑solving, and decision‑making skills with a focus on risk mitigation and value optimization. Commitment to promoting safety, quality, sustainability, and compliance in all project activities. Competencies Collaboration and teamwork. Process improvement. Effective communication. Results orientation. Analytical thinking and problem solving. Requirements Bachelor’s degree in Engineering, Project Management, or a related discipline; advanced degree (MBA, MS) preferred. Minimum 10+ years of project management experience in the pharmaceutical or life sciences industry, with at least 5 years managing capital project portfolios (>$5M scope). Proven track record of delivering complex projects across multiple geographies (US & Canada) within GMP‑regulated environments. Available to travel to sister Bimeda sites to support projects as directed by EVP Global Strategy & Technical Operations. Meets all deadlines associated with projects as directed, including all reports and documentation as directed. Conforms to all principles of cGMP and to relevant company SOPs. What We Offer Competitive salary. 13 paid holidays. Competitive vacation policy effective upon hire. 5 paid personal care days. Medical, dental, vision, STD & LTD benefits. Defined Contribution Pension plan with employer matching 5%. Employee Assistance Program. At Bimeda we are committed to fostering an inclusive, barrier‑free and accessible environment. Part of this commitment includes arranging accommodations to ensure an equitable opportunity to participate in the recruitment and selection process. If you require an accommodation, we will work with you to meet your needs. Location: Kitchener, Ontario, Canada Salary: $110,000 - $160,000 CAD (2024) #J-18808-Ljbffr