Join Catalent in Adair, ON as a Lead Project Manager and spearhead multiple complex projects in pharmaceutical manufacturing. This onsite role emphasizes technical project management and regulatory compliance. In this role, you will oversee various initiatives, including equipment acquisitions and process validation, ensuring adherence to cGMP standards while managing resources and timelines.

Your ability to drive transparency and communicate effectively with stakeholders will be crucial. Key Responsibilities:
Manage concurrent projects from inception to completion
Ensure alignment with Valuable Manufacturing Practices
Analyze risks and develop robust mitigation plans
Provide regular status updates to stakeholders
Lead project governance meetings and decision-making processes

Requirements:
Bachelor’s degree in a relevant field; advanced degrees preferred
Minimum 5 years of experience in biotech or CDMO operations
Solid project management skills with a technical focus
Knowledge of drug development and quality standards
Excellent stakeholder management and negotiation skills

Join us in elevating pharmaceutical manufacturing standards at Catalent!

📌 Lead Project Manager In Pharmaceutical Manufacturing Strathroy
🏢 Catalent Pharma Solutions
📍 Strathroy