- Responsible for working with Subject Matter Experts (SMEs) to create, improve and present changes to Kite MVP-01 lifecycle documents (ie. Validation protocols, SOP’s, WRK’s, TM’s)
Responsible for administering all aspects of the Quality Management System (QMS) as it relates to deviations and Laboratory investigation / LIRs. You will work with SMEs to get all needed data into the QMS to efficiently and punctually open and close Deviations as required by the QC department.
Investigate, author, and execute corrective actions for deviations as required by the QC department.
Active participant in seeking to make the Manufacturing department better at all aspects of its operations.
QMS expert for the QC department.
Work closely with the cross functional team to facilitate communication and execute process improvements in a timely fashion.
Present work during leadership councils and audits as required by QC.
SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
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