Precision Manufacturing Associate
Summary Implements procedures for the production of oligonucleotides, with a concentration on QC testing of the performance of clinical and research assays. Assists with technical issues, optimization of processes, regulatory compliance, scale-up and troubleshooting. Essential Duties and Responsibilities Performs QC testing of manufactured clinical and research assays. Prepares testing reports according to cGMP regulations and internal guidelines Maintains stocks of raw materials, buffers, lab supplies, etc. Maintains department documentation such as database updates, inventory records, and manufacturing batch records. Provides input to process improvements and assists with the development of new and/or improved manufacturing procedures. Calibrates and maintains lab equipment as required. May provide training and guidance to other personnel. Assists with related special projects, as required. Qualifications Education and/or Experience Preferred Bachelor's degree (B.S.) in a scientific discipline (chemistry, molecular biology, biochemistry or related field) from four-year college or university with relevant industry experience preferably in manufacturing and/or quality control. Preferred experience with real time PCR systems (ABI 7900, 7300, RotorGen or similar).
September 15 on ApplicantPRO