Validation Consultant

Job Description

Open position for a Validation Conseultant for a Cork based Pharmaceutical site, initial 12 month contract with opportunity for further work.

Main Responsibilities:

• Proven experience in process validation requirements on new manufacturing processes, equipment introductions & process changes.
• PQ, OQ, IQ
• Write, execute, and review all validation documents.
• Coordinates and executes validation change control and preparation of protocols and reports
• Prepare summaries of validation testing for regulatory submissions, and present validations to regulatory agencies.
• Apply validation principles to work assignments, reviews and approves documents and resolves problems.

 

Experience/Qualifications:

• Degree qualified in a relevant Engineering or Science discipline
• 3+ years relevant experience.
• Extensive understanding and application of validation principles, concepts, practices, and standards particularly in relation to Process Validation.
• Experience in regulated industry, FDA, ISO, GMP etc

Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.

BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.