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
1. Interim Support to Ensure Ongoing Consistency of Quality of Manufactured Products
2. Project Management
3. Process Management
4. Regulatory Knowledge
5. Risk Management
6. Validation Protocols and Reports
7. Data Analysis & Statistics
8. Automation & Control Systems
9. Software Proficiency
10. Knowledge of Validation Life Cycle
11. Continuous Improvement & Industry Trends
12. Knowledge of Environmental Monitoring
13. Qualification of Systems
REQUIRED
1. Bachelor's or Master's Degree in Chemical Engineering, Pharmaceutical Sciences, Mechanical Engineering, or a Proven Track Record of Pharmaceutical Sector Validation
2. Certifications eg Certified Quality Engineer, (CQE), Validation Professional, (CVP), or Other Relevant Pharmaceutical Validation Certifications are Desirable
3. Experience in the Pharmaceutical Industry is Essential, Especially Validation Processes eg Equipment, Systems, Processes, and Cleaning Validation
4. Prior Experience with GMP (Good Manufacturing Practice) is Essential
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