Qualifications 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 03 years of relevant industrial experience. Shift Hours: Primarily 8am 5pm MonFri occasionally working longer or until 22:30 (23 weeks/year) Beta Lactam required so no known allergy 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 handson 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 initiativetaking ability needed for continuous learning and its applications. Strong desire to succeed and to help others to do the same. Heavily Preferred Experiences: Experience working in a cGMP environment Work coop or internship experience in industry
Responsibilities Providing technical support for sterile manufacturing processes in the form of data analysis troubleshooting problemsolving report writing and shopfloor support Supporting change control implementation Collaborating with crossfunctional teams across levels Learning new processes and procedures Performing shift work as needed (expected to be minimal) 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 review
Comments/Special InstructionsHrushikesh Deshpande
System Location: Manufacturing (Z007) Required
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CWR Type: W2 Required