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Manufacturing Process Engineer

Cincinnati, Ohio, USA💼 Full-time🗓 2026-06-23 → 2026-07-30

Core

Develop, validate, and scale up manufacturing processes for therapeutic and diagnostic products (solids, liquids, semi-solids) ensuring GMP compliance and technology transfer.

Role type

Manufacturing Process Engineer (Process Development & Scale-up)

Builds

Scalable manufacturing processes and validated production methods for clinical, scale-up, and registration batches.

Domain

Pharmaceutical manufacturing / Process Engineering

Deliverable

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

Required skills

GMP compliance, process validation, technology transfer, scale-up activities, project management, root cause analysis, risk assessment, equipment methodology development, documentation writing

Preferred skills

Chemical engineering background, experience with immediate and controlled release dosage forms, leading cross-functional technical projects

Technologies

Microsoft Office Suite, manufacturing/quality systems

Responsibilities

Lead process development and scale-up activities for new and established products; Execute technology transfer between clients and internal teams; Investigate and validate new scientific and equipment methodologies; Manage project documentation and regulatory compliance; Collaborate with analytical, quality, and project management teams to resolve technical challenges

Seniority

Mid-level, hands-on IC

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