Quality Control Specialist
📋 Role Overview & Responsibilities
The position directly supports Vedanta’s in-house cGMP manufacturing capabilities including programs in multiple phases of development.
This role will be focused on supporting environmental monitoring and quality data review, with the opportunity to be involved in other aspects of quality control work.
Perform routine Environmental Monitoring (EM) and help support the EM program.Review contract test lab data, protocols, reports, and quality events (deviations, Out of Specification (OOS) investigations, etc.).Review and revise standard operating protocols (SOP), Certificates of Analysis (CoA), and reports.Participate within the Quality Control (QC) team to meet group and company goals.
Requirements:BS in a scientific disciplineMinimum 1+ years working in a GMP environment and/or QC test lab
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This position is located in Cambridge, MA with potential relocation and sponsorship assistance depending on candidate qualifications.
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