CIP Engineer (Pharmaceutical, Denmark)

Job summary

This role focuses on Cleaning-in-Place (CIP) solutions for pharmaceutical projects, emphasizing technical curiosity and collaboration. The position involves supporting projects from concept to handover, ensuring compliance with GMP standards and operational efficiency.

Qualifications

• Degree in engineering (chemical, mechanical, biotechnology, process engineering, or similar).
• Recent graduates or soon-to-graduate engineers with an interest in CIP systems and pharmaceutical production.
• Basic understanding of GMP principles or a strong motivation to learn.
• Experience from student projects, internships, or project-driven environments is advantageous.

Responsibilities

• Design, specify, and deliver CIP systems across all project phases.
• Define CIP strategies and cleaning concepts in accordance with GMP requirements.
• Prepare and review CIP-related documentation such as PFDs, P&IDs, and technical specifications.
• Optimize CIP systems focusing on cleanability, sustainability, and lifecycle cost.
• Collaborate with automation teams on control strategies and CIP recipes.
• Support FAT, SAT, commissioning, and qualification activities.

Skills

• Curiosity and a solution-oriented mindset.
• Structured approach with a focus on delivering results.
• Customer-oriented and consulting-based approach.
• Effective collaboration on team-based projects.

Education

• Engineering degree in relevant fields.

Tools

• Familiarity with CIP systems, utilities, and process equipment in pharmaceutical contexts.