Job Description

For a large client of us we are seeking a skilled Project Engineer / CQV Engineer (Pharma) to join our growing team in Stein. You will become part of an innovative, collaborative environment dedicated to delivering high-quality engineering solutions within the pharmaceutical industry.
In this role, you will play a key part in the implementation, commissioning, qualification, and validation of critical pharmaceutical equipment and processes. Your work will ensure compliance with GMP and CQV standards, while contributing directly to the safety, efficiency, and quality of pharmaceutical production systems.
Essential Requirements

• Bachelor's or Master's degree in Chemical Engineering, Bioprocess Engineering, or a related technical field
• Minimum 2 years of experience in a similar pharmaceutical or biotechnology engineering role
• Strong expertise in GMP, CQV, and regulatory compliance
• Hands-on experience with qualification and validation activities (IQ/OQ/PQ)
• Solid scientific/technical understanding of pharmaceutical systems and processes
• Fluent in both German and English (written and spoken)

Preferred Requirements

• Experience working on multidisciplinary engineering projects
• Advanced technical skills in process engineering, risk management, or automation
• Familiarity with pharmaceutical equipment, utilities, and manufacturing technologies
• Prior involvement in large-scale CQV projects or greenfield/brownfield facility implementations
• Strong problem-solving abilities, presentation skills, and attention to detail

Practicalities
Start Date: 15 December 2025
Contract Duration: 6 months
Location: Stein, Aargau, Switzerland
Additional: Hybrid working model, competitive salary, supportive team culture, and ample professional development opportunities
Interested?
Interviews and offers can progress quickly. Send your CV to Oluali Titelman at o.titelman@panda-int.com or call +31 (0)20 2044 502 today to secure your spot in the process.

Skills Required