Specify and dimension equipment in compliance with GMP, safety, and regulatory requirements
Develop automation strategies and coordinate interfaces with automation, electrical, and other engineering disciplines
Create and review technical documentation for procurement, commissioning, and qualification (QPL, DQ, IQ, OQ)
Evaluate technical and commercial solutions, support cost estimates, and contribute to investment proposals and business cases
Drive standardisation, best practices, and the implementation of new technologies across the group
Requirements
Degree in Process, Chemical, Mechanical, or Pharmaceutical Engineering (or equivalent technical education)
Minimum 10 years of experience in process engineering, preferably within the pharmaceutical or biotech industry, familiarity in GMP / GAMP environment
Proven experience in the design and implementation of process equipment and systems
Strong understanding of mathematics, science, physics, fluid dynamics, and thermodynamics
High proficiency in MS Office and CAD applications (AutoCAD, SolidWorks or similar)
Strong analytical and problem-solving skills, combined with a hands-on mindset and the ability to work independently and collaboratively in international, cross-functional teams
Willingness to travel up to 30 %
Benefits
Attractive salary and benefits package
Skills development
Various internal and external employee and leadership trainings, trainee programs and digital solutions