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