We are looking for a quality analyst to join our organization at a large pharmaceutical client based out of Andover, MA. This team supports downstream development purification and optimization, mRNA drug substance process activities, and providing support to routine manufacturing operations.
This person will be expected to develop and qualify purification techniques, ensure the proper and timely execution of purification processing, and perform scale-down purifications of biologics using precipitation, depth filtration, ultrafiltration, and chromatography. We are looking for someone with experience in techniques such as mRNA Drug Substance process, UF/DF, Column Chromatograph, and ideally familiar with standard downstream equipment, e.g. AKTAs.
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- Purification process development and troubleshooting experience
- Familiarity with mRNA Lipid nano particle formulation and Final Drug Product (FDP) processes
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.