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Supervisor, Formulation Manufacturing

Cincinnati, Ohio, USA💼 Full-time🗓 2026-09-03 → 2026-09-26

Core

Manage teams in producing oral solid dosage pharmaceutical drugs, ensuring operational excellence and cGMP/FDA compliance.

Role type

Senior IC manufacturing supervisor (pharmaceuticals)

Builds

Oral solid dosage pharmaceutical drugs

Domain

Pharmaceutical manufacturing / CDMO

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

cGMP regulations knowledge, FDA requirements knowledge, production scheduling, team leadership, performance management, safety compliance, problem-solving with data

Preferred skills

Science/Engineering/Chemistry degree, pharmaceutical experience

Technologies

None stated

Responsibilities

Coordinate production schedules and optimize systems to increase capacity, Manage a team of 4-6 supervisors and 50+ technicians, Mentor direct reports and conduct performance reviews, Ensure compliance with cGMPs and government agency standards, Support site audits and inspections, Address critical issues through resource allocation and escalation

Seniority

Senior, hands-on IC with people leadership

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