Irvine Pharmaceutical Services, Inc., are expanding our Biopharmaceutical team and currently have an open opportunity for a Sr. Scientist. Must have extensive theoretical and hands on knowledge of HPLC, GC/MS, ELISA, CE, Gel Electrophoresis, and QPCR. Write SOPs and other internal documentation with minimal input from management and collaborating departments. Will develop experimental design, write necessary documents and execute method development, method validation and other activities within a cGMP environment with minimal input from management and colleagues. Participate in the interpretation of data, collaborate with Quality Control, Quality Assurance, and other departments. Support QA/Regulatory affairs by assembling methodology, and data for submission of regulatory documents and FDA investigations with minimal oversight from department management. Will have scientific and technical ability to organize, coordinate and execute project assignments and interpret results independently. Individual expected to coordinate the activities of a small group of chemists/scientists. Additional job responsibilities may be added as necessary.

This position requires a M.S. Degree in Biochemistry or related field with 6 to 8+ years of experience in the biopharmaceutical development field.