Description
A global pharmaceutical organisation is looking for an experienced Cleaning Validation Specialist to support various investment and compliance projects on one of its biggest production sites.Location: Basel area, Switzerland
Duration: 1-2 years
Role and Responsibilities:
• Supporting the execution and documentation of cleaning validation activities in a high containment solid dose production environment (formulation of highly active ingredients)
• Hands on development and execution of cleaning validation protocols
• Documenting all cleaning validation activities in a GMP compliant manner
• Review and analysis of cleaning validation test results to write validation summary reports
• Supporting the development and improvement of validation protocols and master plans in line with current regulatory standards
• Identifying deviations in the cleaning procedures on site and ensuring the implementation of robust CAPAs
Requirements:
• Degree educated in scientific or engineering discipline or equivalent experience
• Good German language skills (spoken and written)
• Experience executing and documentation cleaning validation activities within a pharmaceutical or biotech production environment
• Excellent knowledge of FDA and EU GMP requirements
• Knowledge / experience of equipment qualification and process validation
Apply now for this exciting, long term opportunity.