Lead Hand I
Core
Operate, maintain, and coordinate production activities in a sterile pharmaceutical manufacturing environment to ensure quality and safety standards.
Role type
Lead Hand I (Production)
Builds
Sterile injectable cartridges and combination products
Domain
Pharmaceutical manufacturing / Healthcare
Required skills
Equipment operation, GMP compliance, documentation management, quality testing (IPQC), shift coordination, troubleshooting, on-the-job training
Preferred skills
Previous leadership experience, continuous improvement project participation
Technologies
GMP documentation systems, batch record systems, AX transaction system
Responsibilities
Coordinate shift changeovers and communicate priorities with other shifts; Perform operator duties and troubleshoot equipment alarms; Ensure supply availability and maintain clean, organized work areas; Coach operators on documentation practices and correct errors; Conduct on-the-job training for new employees; Issue and rectify Quality Assurance deviations; Participate in SOP revisions and continuous improvement initiatives.
Seniority
Entry-level to Mid-level, hands-on IC
