Operations Shift Supervisor
Core
Oversee safe and compliant production of drug product materials in a highly automated pharmaceutical manufacturing environment, leading a team of technicians and ensuring adherence to regulatory standards.
Role type
Shift Supervisor (Pharmaceutical Manufacturing)
Builds
Drug product materials
Domain
Pharmaceutical manufacturing / cGMP regulated environment
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
cGMP knowledge, batch processing operations, team leadership, performance metrics management, regulatory compliance, continuous improvement, stakeholder collaboration, EHS standards adherence
Preferred skills
Subject Matter Expert (SME) capability, technical leadership, strategic implementation
Technologies
Manufacturing control systems
Responsibilities
Supervise and execute pharmaceutical processing activities, lead and develop a team of 4-9 direct reports, plan resources and coordinate training, measure and report key departmental performance metrics, ensure compliance with safety and quality SOPs, manage employee relations and performance reviews, represent the area during regulatory inspections and audits
Seniority
Mid-level Supervisor (3+ years experience)
