Description:
- To support the overall Validation Program by conducting qualifications and preparing and/or executing validation documents. This includes the generation, development, modification, and routing of Validation Protocols, Final Reports, Standard Operating Procedures, and Change Controls. Validation systems are in place and used to control/ guarantee the quality of products.
Responsibilities of the Role:
- Execute-validation documentation in line with the standard approval process/protocols
Minimum Requirements:
Bachelor's Degree in Science/Engineering or a related discipline Experience in pharmaceutical industry with the manufacturing environment At least 2 years in a Validation Department Good working knowledge of manufacturing equipment, process, facility, utilities and computerised system validation Proficiency in MS Office (Word, Excel, PowerPoint and Project management) Ability to interpret and relate validation guidelines and standards for implementation to functional areas Demonstrated ability to provide technical solutions for problems through process knowledge Proficient in the use of structured problem-solving tools such as Process Mapping, Root Cause Analysis, Failure Mode effects analysis, etc.Core Competencies:
Presenting and communicating information Applying expertise and technolog...
19 Sep 2022;
from:
gumtree.co.za