A leading company in the pharmaceutical industry is seeking a Process Validation Specialist to join their team in the Leicestershire area. As the Process Validation Specialist, you will play a pivotal role in defining and executing equipment validation activities, ensuring the seamless integration of new technologies into manufacturing operations.
If you think you are the right match for the following opportunity, apply after reading the complete description.
Work with the Pharmaceutical Development and Operations groups to acquire knowledge and understanding of new technologies required to support site operations.
As Process Owner, take responsibility for introducing new process equipment, defining and executing equipment operating procedures, completing data integrity assessments, and developing training packages for Manufacturing Process Development (MPD).
Ensure timely execution of activities in accordance with project strategies, maintaining effective communication with departments such as Manufacturing, Formulation Development, Analytical Support/QC, QA, Scheduling, Project Management, Validation, Stores, and Engineering.
Relevant degree in a related field.
A working knowledge and practical experience with ERP systems and common office applications (Word, Excel, etc.).
Senior Technical Specialist / Equipment Validation / Process Validation / GMP / Pharmaceutical / Process Owner / Manufacturing Operations / Data Integrity / ERP Systems / Technical Investigations / Qualification Lifecycle
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