Repligen is an innovative life sciences company focused on developing and commercializing high-value bioprocessing products, technologies, and solutions critical in the production of biologic drugs.
We are currently seeking a QA Associate I to join our Quality team in Marlborough.
The successful candidate will be responsible for assisting the QA department to revise/create, file, organize, and review production documents. The candidate will work closely with the manufacturing team and document control department to ensure the changes are accurate and are made effective in a timely manner. This position involves completing the QA review of production records, including verification of raw materials used, verification of calculations, critical process steps, and evaluation of Factory Acceptance testing (FAT).
The QA Associate I will actively participate in the Repligen ISO 9001 Quality Management System and will be responsible for the review of system batch records and binder builds for Xcell ATF and Systems product lines and other TFF and TFDF systems.
Responsibilities:
Requirements:
Excellent Benefits!
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