Project Manager Generalist | Life Science

Capgemini Engineering; Diegem; Sur place; EUR 60 000 - 90 000; Plein temps

Avantages offerts par ce poste

Well-being Hub

Career acceleration programs

Mentoring programs

Résumé du poste

Capgemini Engineering in Belgium is seeking an experienced Project Manager Generalist to lead and coordinate strategic and operational projects across pharmaceutical, biotechnology, medical devices, and healthcare sectors.

Join a role where you interface with business, technical, quality and regulatory teams to deliver on time, within scope, and in compliance with GMP/GxP; French language skills are valued.

Qualifications

• 3+ years of PM experience in Life Sciences sectors.
• Experience coordinating cross-functional projects involving QA, Regulatory, Manufacturing.
• Knowledge of GMP/GxP environments.
• Strong stakeholder management and communication skills.
• French fluency; English is a plus.

Responsabilités

• Managing end-to-end project delivery across pharmaceutical, biotechnology, medical device, and healthcare environments
• Coordinating cross-functional teams including R&D, Manufacturing, MSAT, Quality Assurance, Quality Control, Regulatory Affairs, Supply Chain, and Engineering
• Developing and maintaining project plans, timelines, budgets, resource allocation, and risk management strategies
• Ensuring compliance with applicable regulatory requirements, GMP, GxP, and quality standards throughout project execution
• Leading governance meetings, tracking project performance, and providing clear communication to stakeholders and senior management
• Driving technology transfer, process improvement, digital transformation, validation, or operational excellence initiatives depending on project needs
• Identifying project risks, managing issue resolution, and implementing mitigation actions to ensure successful outcomes
• Supporting organizational change management and fostering collaboration across global and multidisciplinary teams

Connaissances

Life Sciences domain knowledge

Project management

Stakeholder management

Regulatory compliance

Cross-functional coordination

GMP/GxP familiarity

Communication skills

French fluency

Formation

Bachelor's degree in Life Sciences or Engineering

Outils

PMP/PRINCE2

Agile

Description du poste

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.

Responsibilities

• Managing end-to-end project delivery across pharmaceutical, biotechnology, medical device, and healthcare environments
• Coordinating cross-functional teams including R&D, Manufacturing, MSAT, Quality Assurance, Quality Control, Regulatory Affairs, Supply Chain, and Engineering
• Developing and maintaining project plans, timelines, budgets, resource allocation, and risk management strategies
• Ensuring compliance with applicable regulatory requirements, GMP, GxP, and quality standards throughout project execution
• Leading governance meetings, tracking project performance, and providing clear communication to stakeholders and senior management
• Driving technology transfer, process improvement, digital transformation, validation, or operational excellence initiatives depending on project needs
• Identifying project risks, managing issue resolution, and implementing mitigation actions to ensure successful outcomes
• Supporting organizational change management and fostering 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.

• A 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
• A 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 – The global Well-Being Hub connects employees across various facets of well-being: work-life balance, working hours and network growth.
• Career acceleration programs – From associate to leaders and beyond, get support in your career at every stage with award-winning programs such as our leadership development program, Connected Manager, to accelerate your growth and develop your expertise.
• Mentoring programs – Capgemini empowers women at all career stages with programs spanning STEM education to career reentry. We value mentorship for fostering professional growth and empowerment within our engineering community.