Product Development Operations Supervisor
Core
Supervise daily Pharmaceutical Development and Clinical Manufacturing operations for oral solid dose development, clinical trial material manufacture, scale-up, and registration batches.
Role type
Senior IC manufacturing operations supervisor
Builds
Clinical trial materials, scale-up batches, and registration support batches for oral solid dosage forms
Domain
Pharmaceutical manufacturing (oral solid dose)
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Team leadership, cGMP compliance, batch record management, cross-functional coordination, equipment setup and changeover, deviation investigation, process validation support, safety protocol enforcement
Preferred skills
Oral solid dose operations, clinical trial material manufacturing, scale-up, technical transfer, process validation, potent compound handling, controlled substance handling, CDMO environment experience
Technologies
Blending, milling, granulation, fluid bed processing, compression, encapsulation, coating equipment
Responsibilities
Plan and supervise pharmaceutical development and clinical manufacturing activities; lead daily production execution ensuring document accuracy and cGMP compliance; provide direct supervision, coaching, and training for production team members; coordinate daily priorities with cross-functional teams; ensure manufacturing suites and equipment are maintained in a state of readiness; supervise equipment set-up, cleaning verification, and batch execution; support development, engineering, and validation protocols; resolve safety, compliance, and execution issues
Seniority
Senior, hands-on IC