This is a temporary position that will be filled for 8 months, but could be extended longer based on employee’s performance.
Perform routine laboratory tasks including reagent preparation, sample management, instrument maintenance, inventory/ordering of supplies, general housekeeping, and other duties as assigned.
Perform non-GMP analytical testing of study samples to support upstream and downstream process development studies.
Document experimental data and results, perform data verification, prepare protocols and final reports.
Support analytical initiatives including method development, qualification, and technical transfer of methods to the Quality Control laboratory.
Collaborate with cross functional teams and assist with troubleshooting.
Occasional night and weekend hours may be required.
Qualifications
Strong written and verbal communication skills.
Detail oriented with good organizational skills.
Knowledge of a variety of analytical biochemistry techniques (i.e., HPLC, qPCR, ELISA, CE-SDS, iCIEF, UV, MS, Cell based assays) is preferred.
B.S./M.S./or Ph.D. in Biology, Chemistry, Biotechnology or equivalent area of related study with 0-5 yrs. relevant experience.
