Pharma Plant Project Engineer III - Sterile GMP CDMO

Energy Jobline ZR; Spokane (WA); On-site; USD 117,000 - 143,000; Full time

Benefits offered by this job

Relocation package

H1B visa transfer

Excellent benefits starting Day 1

Medical

Vision

Dental

Paid time off

401k match

Job summary

Energy Jobline ZR is seeking a Pharmaceutical Plant Project Engineer III for our Spokane, WA site, a cGMP environment supporting sterile and vial manufacturing. You will lead large-scale facility projects and multi-disciplinary teams, providing engineering direction and ensuring regulatory compliance.

The role requires a BS in Engineering, 7+ years in project management, 3+ years in BioPharma, and proficiency in MS Office, AutoCAD, and SAP.

Qualifications

• Bachelor's degree in Engineering or related technical field.
• 7+ years of engineering project management or project engineering experience.
• 3+ years of engineering experience in the BioPharma industry.
• Facility or manufacturing engineering experience.
• MS Office suite (Word, PowerPoint, Excel) experience.
• Ability to work through ambiguity, influence outcomes, and lead cross-functional teams without direct authority.

Responsibilities

• Provide technical support for facility projects including expansions, upgrades, and construction.
• Develop and manage specifications and RFQs for engineering projects.
• Ensure regulatory compliance for facility and processes across applicable agencies.
• Lead multi-departmental project teams and manage schedules and budgets.
• Develop engineering documentation in line with SOPs and quality standards.

Skills

7+ years Project Management experience

3+ years BioPharma industry experience

MS Office proficiency

Strong leadership without authority

Education

Bachelor's of Science in Engineering or related technical degree

BS in Mechanical, Chemical, Electrical or Manufacturing Engineering

Tools

MS Project

AutoCAD

SAP

Job description

Energy Jobline ZR is seeking a Pharmaceutical Plant Project Engineer III for our Spokane, WA site, a cGMP environment supporting sterile and vial manufacturing. You will lead large-scale facility projects and multi-disciplinary teams, providing engineering direction and ensuring regulatory compliance.

The role requires a BS in Engineering, 7+ years in project management, 3+ years in BioPharma, and proficiency in MS Office, AutoCAD, and SAP.