Project Engineer (CAPA / Non-conformances) | Pharmaceutical
At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s most innovative companies unleash their potential. From autonomous cars to life-saving robots, our digital and software technology experts think outside the box as they provide unique R&D and engineering services across all industries. Join us for a career full of opportunities. Where you can make a difference. Where no two days are the same.
Job Description
As a Project Engineer (QA) within the Creams & Liquids production environment, you will be the bridge between Quality Assurance and Operations, ensuring compliance and continuous improvement across pharmaceutical manufacturing processes.
In this role you will play a key role in:
- Leading and coordinating quality-related investigations linked to manufacturing of creams, gels, ointments, lotions, and liquid topical products, including root cause analysis using methodologies such as 5 Whys, Ishikawa, and DMAIC.
- Defining, documenting, and implementing Corrective and Preventive Action (CAPA) plans while collaborating with cross-functional stakeholders to execute measures and verify effectiveness.
- Working within established Quality Management Systems to prepare, update, and review high-quality GMP documentation including investigation reports, risk assessments, and SOP revisions.
- Engaging directly with operators and manufacturing teams on the shop floor to lead fact-finding sessions, collect data during production steps, and coach teams on deviation prevention.
- Managing quality-related projects across multiple departments (Manufacturing, QA, QC, Engineering) while driving alignment and transparency in investigation progress.
Your profile
- 2+ years of experience in pharmaceutical industry, preferably in Quality Assurance, Quality Control, or manufacturing engineering roles.
- Demonstrated experience with QA investigations, CAPA management, deviation handling, and GMP documentation.
- Strong understanding of Quality Management System tools (TrackWise, Veeva, ETQ, Comet or equivalent platforms).
- Knowledge of semi-solid and liquid pharmaceutical manufacturing processes including mixing, homogenization, and filling operations.
- Excellent technical writing skills with the ability to prepare clear, concise, and compliant quality documentation.
- Strong organizational and project management capabilities with the ability to drive cross-functional collaboration and meet established timelines.
What you'll love about working here
- Empowering environment: Autonomy and Goal setting are among the top scores with 8,4+ ratings in our monthly employee feedback Pulse.
- Hybrid working: We encourage flexibility when it comes to when and where works gets done. Employees work with their managers to determine an arrangement that works best for their role and personal circumstances.
- Free access to learning platforms: Free access for all to world-class learning assets and curated programs from Harvard Business Review, Coursera, Pluralsight, Udemy, Microsoft, AWS, Google and many more.
Capgemini is a global business and technology transformation partner, helping organizations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end-to-end services and solutions leveraging strengths from strategy and design to engineering, all fueled by its market leading capabilities in AI, generative AI, cloud and data, combined with its deep industry expertise and partner ecosystem.
Diegem, BE