Your Role
We are looking for an experienced Project Manager Generalist to join our team. In this role, you will lead and coordinate strategic and operational projects within the pharmaceutical, biotechnology, medical devices, and healthcare sectors. You will act as a key interface between business, technical, quality, and regulatory teams, ensuring projects are delivered on time, within scope, and in compliance with industry regulations.
You will play a critical role in driving innovation, operational excellence, and regulatory compliance across a diverse portfolio of Life Sciences projects.
Key Responsibilities
- Manage end-to-end project delivery across pharmaceutical, biotechnology, medical device, and healthcare environments.
- Coordinate cross-functional teams including R&D, Manufacturing, MSAT, Quality Assurance, Quality Control, Regulatory Affairs, Supply Chain, and Engineering.
- Develop and maintain project plans, timelines, budgets, resource allocation, and risk management strategies.
- Ensure compliance with applicable regulatory requirements, GMP, GxP, and quality standards throughout project execution.
- Lead governance meetings, track project performance, and provide clear communication to stakeholders and senior management.
- Drive technology transfer, process improvement, digital transformation, validation, or operational excellence initiatives depending on project needs.
- Identify project risks, manage issue resolution, and implement mitigation actions to ensure successful outcomes.
- Support organizational change management and foster collaboration across global and multidisciplinary teams.
Your Profile
We are looking for a proactive and results-oriented project management professional with a strong understanding of the Life Sciences industry and its regulatory environment.
- Minimum of 3 years of experience in project management within the pharmaceutical, biotechnology, medical devices, healthcare, or related Life Sciences sectors.
- Proven experience managing cross-functional projects involving quality, regulatory, manufacturing, engineering, supply chain, or product development activities.
- Solid understanding of GMP/GxP environments and the challenges associated with regulated industries.
- Strong stakeholder management skills and the ability to influence and coordinate teams without direct authority.
- Experience managing project schedules, budgets, resources, and risks in complex organizational environments.
- Excellent analytical, problem-solving, and decision-making capabilities.
- Strong communication and presentation skills, with the ability to engage effectively with technical and non-technical stakeholders.
- Fluency in French; additional languages such as English are considered a strong asset.
- PMP, PRINCE2, Agile, Lean Six Sigma, or similar certifications are considered an advantage.
What You'll Love About Working Here
- Well-being Hub connecting employees across work-life balance, working hours, and network growth.
- Career acceleration programs supporting growth and expertise development.
- Mentoring programs supporting professional growth and empowerment within the engineering community.