On-Site Project Engineer II – GMP Manufacturing & Validation

Padagis; Minneapolis (MN); On-site; USD 75,000 - 95,000; Full time

Benefits offered by this job

Annual incentive bonus

Long-term incentive bonus plans

Robust employee benefits package

Job summary

Padagis in Minneapolis is seeking a Project Engineer II to lead capital projects in a GMP-regulated pharmaceutical environment. You will manage projects from inception to completion, ensuring compliance with operational and regulatory standards, while working cross-functionally.

The ideal candidate possesses a Bachelor's degree in engineering and 3-6 years of capital project experience. This full-time role offers competitive salary, annual bonuses, and a comprehensive employee benefits package.

Qualifications

• 3-6 years of experience executing capital projects in manufacturing environments.
• Experience in pharmaceutical or regulated environments preferred.

Responsibilities

• Lead projects from concept through commissioning.
• Define project scope, schedule, budget, and resource requirements.
• Manage vendors and ensure successful project delivery.
• Oversee installation, commissioning, and troubleshooting of equipment.
• Provide technical guidance on process and system improvements.

Skills

Capital project management

Vendor management

Risk identification and mitigation

FDA and GMP compliance

Process optimization

Education

Bachelor's degree in engineering

Job description

Padagis in Minneapolis is seeking a Project Engineer II to lead capital projects in a GMP-regulated pharmaceutical environment. You will manage projects from inception to completion, ensuring compliance with operational and regulatory standards, while working cross-functionally.

The ideal candidate possesses a Bachelor's degree in engineering and 3-6 years of capital project experience. This full-time role offers competitive salary, annual bonuses, and a comprehensive employee benefits package.