JOB PURPOSE:
Supervises Manufacturing Associates, schedules shift tasks, ensures cGMP compliance and safety procedures are adhered to. Ensures manufacturing documentation is updated and revised accordingly. System expert who can lead technical resolution and troubleshooting while representing MFG in cross functional teams.
Responsible for managing and developing direct reports. Can step in to fill in for manager when necessary. Understands department needs and capabilities well.
MAIN ACCOUNTABILITIES:
Schedules and directs daily manufacturing activities, timely communicating scheduling changes/issues to their staff and management.
Hires and develops a well-functioning team - focusing on values and culture.
Trains Manufacturing Associates on process activities, including Safety and CGMP requirements.
Ensure establishment of goals and development plans for employees.
Coordinates and drafts revisions to automated batch documents.
Coordinates manufacturing activities with other department as well as other sites; provides updates to production schedulers and works closely with quality, materials management, manufacturing science, validation, facilities, process engineering etc.
Supervises validation activities, ensuring proper and timely execution of validation protocols required in the areas.
Biotech or pharmaceutical BSc degree or other relevant educational background from chemical industry, food industry, pharmaceutical or biotech industry.