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Validation and Compliance Manager

3 weeks ago


Jersey City, New Jersey, United States Kasmo Global Full time
Job Summary

We are seeking a highly skilled Validation Specialist to join our team. The ideal candidate will have a strong background in commissioning, qualification, validation, and maintenance activities within aseptic manufacturing or cell therapy environments.

The successful candidate will oversee multiple CQV projects, providing updates and coordinating with internal teams and external vendors.

This role requires a strong understanding of cGMP regulations, FDA/EU guidelines, and Good Tissue Practices (cGTP). Experience working with batch records, SOPs, CQV protocols, and technical documentation is also essential.