Reporting to the Director of GMP Quality Assurance Operations, this position will responsible for management of Quality documents and records, administering Veeva electronic document management system, conducting Quality checks on QA and other critical department records as required, managing the training program, developing compliant Quality documentation systems and procedures as needed, and building the QAD staff as needed. This is a full-time position located in Cambridge MA.
The position will be responsible for the following functions:
If interested and qualified, please include Requisition # 2018-367 in the subject line when emailing resume to: firstname.lastname@example.org.
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