Senior Pharma Facility Project Engineer — Lead & Impact

Jubilant HollisterStier LLC; Spokane (WA); On-site; USD 103,000 - 165,000; Full time

Benefits offered by this job

Benefits start day one

FSA/HSA

Life Insurance

AD&D Insurance

Disability Insurance

Employee Assistance Program

Job summary

Jubilant HollisterStier LLC in Spokane, WA, is seeking a Senior Project Engineer to lead large-scale pharmaceutical facility projects. You will provide technical direction, manage multi-disciplinary teams, and ensure compliance with cGMP, USP and global standards across local and international operations.

The role focuses on designing and optimizing manufacturing processes, overseeing existing workflows, and driving continuous improvement through data-driven methods.

Qualifications

• BS degree in Mechanical, Chemical, Bioengineering, or similar engineering field.
• 5–10 years of related pharmaceutical or FDA-regulated experience.
• Supervisory or other leadership experience.
• Project management experience.
• Lean Six Sigma preferred.
• Aseptic manufacturing preferred.
• Fill finish experience preferred.
• Microsoft Office proficiency.

Responsibilities

• Provide expert technical support for facility projects including expansions, upgrades, and compliance efforts.
• Design, optimize and implement site manufacturing processes for efficiency and quality.
• Oversee and assess existing processes and workflows.
• Establish and track process metrics for stability and improvement.
• Manage cGMP, USP and global regulatory compliance across facilities.
• Lead end-to-end product life cycle management from quotation to retirement.
• Develop and execute validation studies for processes.
• Generate reports documenting study results and data.

Skills

Project management

Leadership

Communication

Regulatory liaison

Data analysis

Problem solving

Education

BS in Mechanical, Chemical, or Bioengineering

Tools

Microsoft Office

Job description

Jubilant HollisterStier LLC in Spokane, WA, is seeking a Senior Project Engineer to lead large-scale pharmaceutical facility projects. You will provide technical direction, manage multi-disciplinary teams, and ensure compliance with cGMP, USP and global standards across local and international operations.

The role focuses on designing and optimizing manufacturing processes, overseeing existing workflows, and driving continuous improvement through data-driven methods.