Project Manager Design Transfer Quality Control for Diagnostic Products | Projektleiter (m/w/d) Design Transfer Qualitätskontrolle von Diagnostikprodukten in München (1644)

Brüggen Engineering GmbH

München, Bayern, Deutschland
Published Mar 12, 2026
Full-time
Permanent

Job Summary

This role involves taking a key leadership position within the quality control environment of diagnostic products in Munich. As a Project Manager for Design Transfer QC, you will be responsible for the seamless transition of new or modified diagnostic products from the development phase into routine testing. Your daily activities will include milestone planning, establishing robust QC processes, and ensuring all procedures meet strict GMP and regulatory standards. You will lead interdisciplinary project teams in a matrix structure, coordinating with global interfaces to ensure timely product releases. A significant part of the role focuses on process optimization through 'Go-Lean' activities and supporting regulatory submissions and audits. This position is ideal for professionals with a strong scientific background who enjoy high-stakes documentation and technical problem-solving. It offers a unique opportunity to work at the intersection of innovation and safety, contributing directly to patient benefits within a highly regulated and stable industry.

Required Skills

Education

Completed university degree in natural sciences (e.g., Chemistry, Biology, Biochemistry); a Doctorate (PhD) is preferred.

Experience

  • Several years of professional experience in project management, design transfer, or quality control within a GMP-regulated environment
  • Proven experience in creating and maintaining GMP-compliant documentation and reports
  • Experience in coordinating interdisciplinary project teams and working with global interfaces
  • Experience in process optimization and efficiency improvement (Lean activities)
  • Experience with laboratory diagnostics or analytical equipment is preferred

Languages

German (Fluent)English (Fluent)

Additional

  • The role requires a secure handling of SAP and standard Office tools. Candidates must be prepared to work in a highly regulated environment involving IVDR and ISO standards and support authority audits.