You will be responsible for:

• Manufacturing of Concentrates, Purified Antibodies, and Purified Conjugates via liquid chromatography

• Auditing and GMP/GDP verification of batch records and product release responsibilities.

• This position includes the handling of all types of materials, including hazardous and DEA (Drug Enforcement Agency) controlled materials.

Your role:

• Following established manufacturing protocols to conjugate and/or isolate proteins for use in immunological assays.

• Buffer and chromatography column preparation

• Maintaining a legible and accurate batch record according to proper GMP

• Making decisions and executing critical steps in the manufacturing process

• Maintaining an FDA/DEA compliant laboratory

• Providing Quality Notification Support

• Executing temporary manufacturing deviations and pilot products

• Completion of all necessary training activities