As a Qualification Specialist, you will play a pivotal role in ensuring the ongoing validation and compliance of equipment, systems, and processes at a leading bio-pharmaceutical company.
Main Responsibilities:
* Coordinate designing, executing, and reporting on periodic qualification programs to ensure seamless system integration
* Designing, executing, and reporting on periodic requalification studies for equipment, systems, and processes to maintain high operational standards
In this challenging yet rewarding role as a Qualification Specialist, you will be responsible for evaluating technical knowledge of pharmaceutical plants. You must have an understanding of current regulations regarding Good Manufacturing Practices (GMPs) and regulatory requirements.