Location: Remote with occasional travel to MA
Duration: 6+ Months
Start Date: ASAP
Our Client is looking for a Consultant for a 6 plus month project. This Consultant will be doing the Quality Oversight of CSV for the site. Will be writing and executing protocols, test scripts, and documents (updating procedures) for the group. The work is all oversight of CSV from a Quality perspective. Group is technical operations and handles batch record review documentation. They are switching over from a paper based batch record system to electronic batch records. They use Kneat to manage validations. Will do some digital validation on the floor when onsite.
10+ years of CSV experience with a recent emphasis on Quality oversight. Syncade experience is required but no coding. Pharmaceutical/Biotech experience is required and any Kneat background would be a plus.
Most Important Skills: Quality Oversight of CSV, Review/Approvals of CSV Documentation, Syncade, Review/Approval of test scripts, Manufacturing, Pharmaceutical, Biotech
Quality Oversight Of CSV (232678) Remote MA
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