PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to clients in the pharmaceutical, nutritional and related sectors. With offices across Europe, Asia and the US, our focus is on consistently delivering high‑quality outcomes for multinational clients. We have over 20 years of experience in delivering consistent quality results.

• Support Cleaning Validation activities within a GMP BioPharma manufacturing environment.
• Develop, execute, and maintain Cleaning Validation protocols, reports, and lifecycle documentation.
• Perform risk assessments, residue limit calculations, and sampling strategy development.
• Execute swab and rinse sampling activities for manufacturing equipment and process systems.
• Ensure compliance with FDA, EMA, GMP, and internal quality standards.