Provide technical support for sterile manufacturing processes through data analysis, troubleshooting, problem-solving, report writing, and shop-floor support.
Support change control implementation.
Collaborate with cross-functional teams across various levels.
Learn and adapt to new processes and procedures.
Perform shift work as needed (expected to be minimal).
Conduct technical investigations and analyses.
Recommend and implement corrective and preventative actions, contributing to the reduction of atypical events.
Write, review, and improve procedures for the operation of equipment and processes.
Contribute to process and equipment safety reviews.
Qualifications and Required Skills:
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.
0-3 years of relevant industrial experience.
Shift Hours: Primarily ~8:00 AM – 5:00 PM Monday–Friday, occasionally working longer hours or until 10:30 PM (~2-3 weeks/year). Beta Lactam requirement applies (candidates must not have known allergies).
Excellent academic record.
Strong verbal and written communication skills, teamwork abilities, personal character, and ethics.
Proficiency in problem-solving with a hands-on approach, including a preference for direct field observation.
Ability to assess issues from diverse perspectives (e.g., safety, compliance, maintenance, automation, equipment, process, and people) for optimal resolution.
Enthusiasm, confidence, and proactive learning capability.
A strong desire to succeed and help others achieve success.
Heavily Preferred Experiences:
Experience working in a cGMP environment.
Work, co-op, or internship experience in the industry.
