High school diploma or GED
At least 2 years of leadership, lead or supervisory experience in a regulated manufacturing environment.
Experience in aseptic processing, sterile manufacturing, pharmaceutical, biotechnology or medical device production, with working knowledge of cGMPs, quality systems and manufacturing documentation practices.
Experience using production metrics to support operational improvements and proficiency with Microsoft Office and manufacturing systems.
Ability to work flexible schedules, including weekends, overtime and off-shifts, based on business needs.
Stand, walk, bend, reach and perform repetitive hand movements throughout the workday.
Lift up to 40 pounds occasionally.
Wear required personal protective equipment and comply with cleanroom gowning requirements, including sterile gowns, gloves, masks and hair coverings.
Work regularly in GMP-regulated manufacturing and classified cleanroom environments.
Successfully complete gowning qualifications and follow aseptic techniques and contamination-control procedures.
Support multiple shifts, including days, nights, weekends and overtime, based on business needs.