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...