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SalaryQualifications:
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
Responsibilities:
- 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
