Job Description:
We are currently seeking a skilled Validation Specialist to join our team. This is an exciting opportunity to work with a leading organization in the pharmaceutical industry.
The successful candidate will be responsible for executing cleaning cycle development and PQ of equipment, writing and adhering to validation strategies, coordinating with outside vendors, writing protocols independently, sample submission, analyzing test results, and preparing technical reports.
This role requires strong problem-solving skills, attention to detail, and excellent communication skills. The ideal candidate will have experience as a validation specialist in a pharmaceutical or highly regulated environment and a B.Sc. Degree or other qualification in Chemical Engineering, Biochemistry, Microbiology, Chemistry, or a related field.
In addition to these requirements, the candidate should have experience in at least three of the following areas: C&Q validation, Cleaning Validation, Equipment validation, Process operations, or manufacturing, Process Engineering. A working knowledge of GxP systems associated with this role would be advantageous.