Project Engineer Site Technical Services (MDCP)
Life Sciences
Validation and Qualification
Master
Advanced (5+)
- Location
- Puurs-Sint-Amands, Antwerp
- Work type
- Consultancy
- Work model
- Fulltime, On-site
Our client, a leading pharmaceutical organization, is seeking a technical expert to provide project-driven support for robust manufacturing operations. This role focuses on sustaining on-market medical devices and combination products through technical improvements, process changes, and risk management activities. The position acts as a bridge between production and R&D to facilitate product launches and ensure continuous improvement.
Responsibilities
- Lead and support technical improvement and investment projects from scoping and planning to execution.
- Investigate delivery system customer complaints to determine root causes and implement effective CAPA.
- Drive process and system enhancements with a focus on Design History File (DHF) updates and risk management.
- Prepare and execute technical documentation including protocols, reports, and impact assessments for design and process changes.
- Coordinate with cross-functional teams and external suppliers to ensure on-time delivery and clear communication.
- Support quality assurance in the disposition of non-conforming reports and the qualification of materials or processes.
- Identify and communicate technical risks while developing appropriate mitigation strategies for stakeholders.
Requirements
- You have a Master’s degree in Mechanical, Biomedical, Chemical, or Manufacturing Engineering.
- You have 3+ years of experience in project engineering or technical support within the pharmaceutical or medical device sector.
- You bring expertise in quality and technical standards including GMP, CAPA, and root cause analysis.
- You possess project management capabilities covering planning, prioritization, and stakeholder engagement.
- You are proactive, detail-oriented, and possess strong analytical problem-solving skills.
- You are fluent in English with knowledge of Dutch considered a plus.
Nice to Haves
- Knowledge of 21 CFR Part 820, ISO 13485, and ISO 14971 standards.
- Experience with injection molding technologies pertaining to the medical device industry.
- Direct experience with Medical Device and Combination Product (MDCP) technology.
Offer
- Enjoy a competitive salary package with extra perks that recognize your talent.
- Advance your career with a clear growth path, coaching, and mentoring to support you.
- Thrive in a dynamic and supportive environment where you can truly make an impact.
- Work when and where you perform best, ensuring an optimal work-life balance.
- Choose a flexible transport solution, from a company car to a public transport subscription.
- Expand your network and enjoy unforgettable moments at exclusive events and afterworks.
- Grow your skills with external courses and our in-house Pauwels Academy.
- Work on exciting projects with industry leaders in Life Sciences, Engineering & Digital.
- Seize opportunities at every level, from a strong start to career acceleration and expert collaboration.
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