Minimum of 4+ years of experience in a cGMP manufacturing environment with a High School Diploma/GED
OR 2+ years of cGMP manufacturing experience with an Associate degree in Life Sciences, Engineering, or a related technical discipline
OR a Bachelors degree in Life Sciences, Engineering, or a related technical discipline
OR equivalent military training or experience
Experience working within a GMP-regulated biologics, biotechnology, or pharmaceutical manufacturing environment.
Knowledge of cGMP regulations and safety requirements applicable to biologics and pharmaceutical manufacturing environments.
Familiarity with automated manufacturing control systems, such as Distributed Control Systems (DCS) and Manufacturing Execution Systems (MES).
Experience with electronic batch records and electronic manufacturing systems.
Experience operating bench-scale or large-scale bioreactors and associated upstream equipment.
Comfort working in a structured, procedure-driven environment with strict documentation and compliance expectations.
Ability to support a 24/7 manufacturing facility and work a rotating night shift schedule.
Ability to perform fermentation, sampling, and upstream processing activities, including operation of bioreactors and single-use systems.
Lifting materials up to 33 pounds
The role is physically active and involves standing for extended periods, performing repetitive tasks with hands, wrists, and fingers, bending, pushing, pulling, reaching, lifting materials up to 33 pounds, and ascending ladders to access manufacturing equipment.
The environment may involve temperature-variable conditions and requires the use of personal protective equipment, including respiratory protection when necessary.