Engineer I

•Providing technical support for vaccine, biologic, and sterile manufacturing processes in the form of data analysis, troubleshooting, problem-solving, report writing •Supporting change control implementation •Learning new processes and procedures •Performing shift work as needed •Conducting technical investigations and analyses •Recommending and implementing corrective and preventative actions, and helping lead reduction of atypical events •Writing, reviewing, and improving procedures for operation of equipment and processes •Contributing to process and equipment safety reviews Quals Education and Experience Requirements: •B.S. or M.S. degree in, biology, biochemistry, biochemical engineering, biological systems engineering, biomedical engineering, chemical engineering, computer science, integrated science, or related disciplines and 0-3 years of relevant industrial experience. •Shift Hours: Rotating 12 Hour Shift (6am - 6pm or 2pm-2am; 7 days a week) The successful candidate must have: •Excellent academic record •Strong verbal and written communication skills, team skills, personal character, and ethics •Strong problem solving skills and a hands-on approach to problem solving, with a bias towards going to see problems for oneself in the field. •Ability to examine an issue from diverse perspectives (safety, compliance, maintenance, automation, equipment, process, and people) in order to best understand and resolve it. •Enthusiasm, confidence, and initiative-taking ability needed for continuous learning and its applications. •Strong desire to succeed and to help others to do the same. Preferred Experiences: •Experience working in a cGMP environment •Work, co-op, or internship experience in industry