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.
Working knowledge of cGMPs, quality systems, and manufacturing documentation practices.
Experience using production metrics to support operational improvements.
Proficiency with Microsoft Office and manufacturing systems.
Ability to work flexible schedules, including weekends, overtime, and off-shifts as needed.
Ability to stand, walk, bend, reach, and perform repetitive hand movements throughout the workday.
Ability to lift up to 40 pounds occasionally.
Must be able to wear required PPE and comply with cleanroom gowning requirements, including sterile gowns, gloves, masks, and hair coverings.
Must successfully complete gowning qualifications and follow aseptic techniques and contamination control procedures.
Flexibility to support multiple shifts, including days, nights, weekends, and overtime based on business needs.
