Project Manager – Pharmaceutical Industry

Nalys; Brussel; Sur place; EUR 70 000 - 90 000; Plein temps

Résumé du poste

A leading consultancy firm in Brussels is seeking a Project Manager to lead strategic projects for new products and technologies in the pharmaceutical sector. The role involves overseeing project lifecycles, managing multidisciplinary teams, and ensuring adherence to cGMP standards. Ideal candidates have a Master's degree, 5+ years of project management experience, and fluency in French and English. Join a dynamic team committed to excellence and innovation.

Qualifications

• Minimum of 5 years experience in project management, ideally in the pharmaceutical industry.
• Experience with sterile production product transfers.
• Fluent in French and English.

Responsabilités

• Manage and coordinate multidisciplinary project teams.
• Define project scope, timelines, and resource plans.
• Monitor project performance and identify risks.
• Ensure compliance with cGMP standards.
• Communicate progress and risks through reports.

Connaissances

Leadership

Stakeholder management

Technical coordination

Communication

Budget forecasting

Formation

Master's degree in Engineering or Biotechnology

Outils

MS Project

Excel

Word

PowerPoint

Description du poste

About Nalys

Nalys is a fast-growing consultancy company specialized in high-tech engineering and life sciences. We partner with leading organizations to deliver innovative solutions and expert support across a wide range of technical domains. At Nalys, we combine deep expertise with a human‑centric approach — empowering our consultants to thrive and our clients to succeed. Joining Nalys means becoming part of a collaborative, agile, and forward‑thinking team that values excellence, innovation, and continuous growth.

Job Description

As a Project Manager, you will lead strategic projects for the introduction of new products and technologies within a major pharmaceutical site near Brussels. Reporting to the Senior Manager, you will oversee the full project lifecycle — from inception to completion — ensuring alignment with timelines, budgets, and quality standards. This role requires strong leadership, stakeholder management, and technical coordination skills to deliver impactful results in a regulated environment.

Your Responsibilities

• Manage and coordinate multidisciplinary project teams, ensuring clear objectives and deliverables
• Define project scope, timelines, and resource plans in collaboration with stakeholders
• Monitor project performance, identify risks, and implement mitigation strategies
• Supervise technical planning, documentation, and compliance with cGMP standards
• Communicate progress, risks, and actions internally and externally through reports and presentations
• Prepare and present updates during workshops and monthly Steering Group meetings
• Ensure cost control, invoicing, and budget forecasting throughout the project lifecycle
• Support on-site activities during manufacturing phases and escalate issues when necessary.

Profile / Requirements

• You hold a Master's degree in Engineering, Biotechnology, or related field
• You have a minimum of 5 years experience in project management, ideally in the pharmaceutical industry
• You already worked in sterile production product transfers
• You act as an expert with cGMP standards
• You communicate fluently in French and English
• You are an excellent communicator
• Proficient in MS Project, Excel, Word, and PowerPoint.

Recruitment Process

By applying to the position of Project Manager, here are the steps you will follow during the recruitment process:
1. Olivia Braszko, our Talent Acquisition Specialist, will review your application and schedule a first screening.
2. For the second interview, you will meet our Technical Director, Alexandre Ivankovich for a deeper discussion.
3. A final interview will be held with our Business Unit Director, Jimmy Rousseaux.