Pharma Manufacturing Engineer — Process Optimization

Sharp Services; United States; On-site; USD 85,000 - 110,000; Full time

Job summary

Sharp Services in the United States is seeking a Manufacturing Engineer to optimize and troubleshoot pharmaceutical manufacturing processes, ensuring safe, compliant, and high‑quality production.

You will lead cross‑functional projects, validate equipment, mentor operators, and drive continuous improvement using Lean Six Sigma in a highly regulated environment. A degree in engineering and 3+ years in pharma manufacturing are preferred, with knowledge of AutoCAD/SolidWorks a plus.

Qualifications

• Bachelor’s degree in engineering or related field; degree in progress considered.
• 3+ years in a manufacturing engineering role, preferably pharma or life sciences.
• Strong knowledge of pharmaceutical manufacturing processes and regulatory requirements (FDA, GMP).

Responsibilities

• Design and optimize processes to improve efficiency, reduce waste, and ensure quality.
• Oversee installation and maintenance of manufacturing equipment per specs and standards.
• Ensure GMP and FDA compliance with accurate records and documentation.
• Author Change Controls and related documentation; review MPRs as needed.
• Collaborate with QA to address root causes and sustain product quality.
• Lead cross-functional process-improvement projects and scale-up activities.
• Train operators and technicians on new processes and safety procedures.

Skills

Process optimization

Regulatory compliance

Cross-functional collaboration

Troubleshooting

Project management

Lean Six Sigma

Safety awareness

Education

Bachelor's degree in Mechanical Engineering

Bachelor's degree in Chemical Engineering

Pharmaceutical Engineering (related field)

Degree in progress

Tools

AutoCAD

SolidWorks

Process simulation tools

Job description

Sharp Services in the United States is seeking a Manufacturing Engineer to optimize and troubleshoot pharmaceutical manufacturing processes, ensuring safe, compliant, and high‑quality production.

You will lead cross‑functional projects, validate equipment, mentor operators, and drive continuous improvement using Lean Six Sigma in a highly regulated environment. A degree in engineering and 3+ years in pharma manufacturing are preferred, with knowledge of AutoCAD/SolidWorks a plus.