Packaging & Process Improvement Engineer II

Scorpion Therapeutics; Michigan; On-site; USD 90,000 - 130,000; Full time

Job summary

Scorpion Therapeutics in Allegan, MI is seeking a manufacturing operations engineer to provide technical expertise and lead improvements on packaging lines and production cells.

You will collaborate with engineering, quality, and operations, drive DMAIC projects, train teams, support capital initiatives from scope to startup, and ensure safety, quality, and regulatory compliance in a fast-paced cGMP environment.

Qualifications

• Bachelor’s degree in Engineering (Mechanical, Electrical, Industrial, Manufacturing, or Engineering Management).
• Strong fundamentals of equipment operation; use standard engineering principles/techniques.
• Ability to read drawings, flowcharts, schematics.
• Demonstrated lean and six sigma understanding; experience with continuous improvement techniques.

Responsibilities

• Review the previous 24 hours of production data on designated work centers and address urgent needs.
• Track line efficiency using Pareto charts and data tracking software.
• Monitor changes to ensure impact and ROI are achieved.
• Coordinate and lead continuous improvement projects using DMAIC.
• Generate data for project scopes, cost estimates, economic justifications, and capital appropriation requests.
• Provide direction as a project manager to allied support groups and interface with departments, consultants, and contractors.

Skills

Lean Six Sigma

DMAIC

Reading drawings

Continuous improvement

Project management

Education

Bachelor’s degree in Engineering

Tools

Data tracking software

Pareto charts

Job description

Scorpion Therapeutics in Allegan, MI is seeking a manufacturing operations engineer to provide technical expertise and lead improvements on packaging lines and production cells.

You will collaborate with engineering, quality, and operations, drive DMAIC projects, train teams, support capital initiatives from scope to startup, and ensure safety, quality, and regulatory compliance in a fast-paced cGMP environment.