Validation Specialist

Well Established Pharmaceutical CMO is Seeking to Add to the Team on a Six-Month Fixed Term Contract Basis, an Experienced Validation Specialist, who Will Work Full Time, On-Site, at a State-of-the-Art Facility in a Highly Conducive Environment ROLE * Interim Support to Ensure Ongoing Consistency of Quality of Manufactured Products * Project Management * Process Management * Regulatory Knowledge * Risk Management * Validation Protocols and Reports * Data Analysis & Statistics * Automation & Control Systems * Software Proficiency * Knowledge of Validation Life Cycle * Continuous Improvement & Industry Trends * Knowledge of Environmental Monitoring * Qualification of Systems REQUIRED * Bachelor’s or Master’s Degree in Chemical Engineering, Pharmaceutical Sciences, Mechanical Engineering, or a Proven Track Record of Pharmaceutical Sector Validation * Certifications eg Certified Quality Engineer, (CQE), Validation Professional, (CVP), or Other Relevant Pharmaceutical Validation Certifications are Desirable * Experience in the Pharmaceutical Industry is Essential, Especially Validation Processes eg Equipment, Systems, Processes, and Cleaning Validation * Prior Experience with GMP (Good Manufacturing Practice) is Essential