Cleaning Validation Engineer

About the role

We are looking for a Cleaning Validation Engineer to support cleaning validation activities in a biologics manufacturing environment. You will develop validation documentation, coordinate execution of cleaning protocols, and investigate cleaning deviations to ensure GMP compliance.

Key responsibilities

• Develop and author cleaning validation protocols and reports in line with GMP and site procedures.
• Coordinate with manufacturing and cross‑functional teams to execute cleaning validation studies, including sampling and documentation review.
• Support troubleshooting and investigation of cleaning deviations, identify root causes and implement corrective actions.
• Ensure all cleaning validation activities meet regulatory and quality requirements.
• Collaborate with QA, Manufacturing, and Engineering to deliver validation deliverables on schedule.
• Maintain and update validation documentation and manage change‑control activities.

Required profile

• 1–3 years of experience in a pharmaceutical or biologics manufacturing environment.
• Prior exposure to cleaning validation preferred.
• Familiarity with GMP regulations and validation documentation practices.
• Experience working with manufacturing teams for protocol execution.
• Strong problem‑solving and investigation skills for deviation handling.
• Effective communication and ability to collaborate across functions.

Required skills

• Cleaning validation
• GMP regulations
• Validation documentation
• Sampling methods
• Root cause analysis
• CAPA processes

What we offer

• Generous leave policy
• Comprehensive health and wellness coverage
• Professional development and continuous learning opportunities