Pharma Project Manager - Cross-Functional & Compliance

St-Amour; Montreal (administrative region); On-site; CAD 90,000 - 120,000; Full time

Job summary

St-Amour is seeking a Project Manager to lead cross-functional pharmaceutical initiatives aimed at operational excellence and regulatory compliance. You will work with Quality, Regulatory Affairs, R&D, Supply Chain, Finance and Commercial Operations to ensure projects meet timelines and budgets.

You will develop project charters, monitor KPIs, and drive continuous improvement across manufacturing and documentation processes, while aligning with cGMP, FDA, Health Canada, EMA and ICH guidelines.

Qualifications

• Experience leading cross-functional pharmaceutical projects.
• Strong stakeholder management and communication skills.
• Familiarity with regulatory requirements and project governance.

Responsibilities

• Lead the execution of high-impact, cross-functional projects across Quality, Regulatory, R&D, Supply Chain, Finance and Commercial Operations.
• Coordinate teams and stakeholders to deliver projects on time and within budget.
• Develop and maintain project charters, timelines, budgets, risk plans and performance indicators.
• Monitor KPIs and project outcomes to drive accountability and continuous improvement.
• Ensure compliance with cGMP, FDA, Health Canada, EMA and ICH guidelines.
• Support process optimization across production workflows and documentation practices.
• Collaborate with Finance, Procurement and Commercial Operations to manage resources and costs.
• Conduct post-project reviews and implement lessons learned for future initiatives.

Skills

Project management

Cross-functional collaboration

Stakeholder management

KPI tracking

Job description

St-Amour is seeking a Project Manager to lead cross-functional pharmaceutical initiatives aimed at operational excellence and regulatory compliance. You will work with Quality, Regulatory Affairs, R&D, Supply Chain, Finance and Commercial Operations to ensure projects meet timelines and budgets.

You will develop project charters, monitor KPIs, and drive continuous improvement across manufacturing and documentation processes, while aligning with cGMP, FDA, Health Canada, EMA and ICH guidelines.