Engineer I

Providing technical support for sterile manufacturing processes in the form of data analysis, troubleshooting, problem-solving, report writing, and shop-floor support

Supporting change control implementation

Collaborating with cross-functional 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



Quals--

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: Primarily ~8am 5pm Mon-Fri, occasionally working longer or until 22:30 (~2-3 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 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.



Heavily Preferred Experiences:

Experience working in a cGMP environment

Work, co-op, or internship experience in industry