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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.
# 93603
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