Project Engineer – Pharmaceutical Capital Projects

Intellectt Inc; Fort Worth (TX); On-site; USD 90,000 - 130,000; Part time

Benefits offered by this job

Health Insurance

401(k) retirement savings

PTO per state law

Job summary

Intellectt Inc. is seeking an experienced Project Engineer to manage capital and engineering projects within a GMP pharmaceutical manufacturing environment in Fort Worth, TX.

Initial projects include packaging line upgrades, blender upgrades, and qualification of a new warehouse facility. You will lead planning, budgeting, installation, commissioning, and handover, while coordinating with Engineering, Manufacturing, and Quality teams to ensure GMP compliance and quality deliverables across the

Qualifications

• Experience managing pharmaceutical capital and engineering projects in a GMP environment.
• Hands-on equipment and facility qualification experience, including IQ/OQ/PQ execution.
• Knowledge of commissioning and process validation.
• Ability to manage multiple projects, budgets, schedules, contractors, and stakeholders.
• Certification: PMP, PgMP, Lean Six Sigma Black Belt, or CMRP.

Responsibilities

• Manage projects from planning and budgeting through installation, commissioning, qualification, and handover.
• Develop and track project schedules, budgets, milestones, and deliverables.
• Coordinate vendors, contractors, and internal Engineering, Manufacturing, and Quality teams.
• Support equipment and facility qualification, including hands-on IQ/OQ/PQ protocol execution.
• Ensure GMP compliance, maintain project documentation, and report progress to site leadership.

Skills

GMP experience

Project management

Cross-functional coordination

IQ/OQ/PQ execution

Budgeting

Education

PMI Certification (PMP/PgMP) or Lean Six Sigma Black Belt or CMRP

Job description

Job Title: Project Engineer - Pharmaceutical Capital Projects

Company: Intellectt

Employment type: Contract

Job Summary

Seeking an experienced Project Engineer to manage capital and engineering projects within a GMP pharmaceutical manufacturing environment. Initial projects include packaging line upgrades, blender upgrades, and qualification of a new warehouse facility.

Key Responsibilities

• Manage projects from planning and budgeting through installation, commissioning, qualification, and handover.
• Develop and track project schedules, budgets, milestones, and deliverables.
• Coordinate vendors, contractors, and internal Engineering, Manufacturing, and Quality teams.
• Support equipment and facility qualification, including hands-on IQ/OQ/PQ protocol execution.
• Ensure GMP compliance, maintain project documentation, and report progress to site leadership.

Required Qualifications

• Experience managing pharmaceutical capital and engineering projects in a GMP environment.
• Hands-on equipment and facility qualification experience, including IQ/OQ/PQ execution.
• Knowledge of commissioning and process validation.
• Ability to manage multiple projects, budgets, schedules, contractors, and stakeholders.
• At least one certification: PMP, PgMP, Lean Six Sigma Black Belt, or CMRP.

Benefits

Employees hired into this position are eligible for the following benefits, subject to the applicable plan terms and eligibility requirements:

Health Insurance

Medical, dental, and vision insurance options are available through a third-party provider. Employees are responsible for paying the full cost of their insurance premiums.

Retirement Benefits

A 401(k) retirement savings plan is available. No employer matching or other employer contributions are provided.

Paid Time Off (PTO)

No PTO other than that required by applicable state and local laws