Project Engineer - GMP Life Sciences & Facilities

biotech

Boulder (CO)

On-site

USD 100,000 - 120,000

Full time

10 days ago
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Benefits offered by this job

Medical premiums coverage
401(k) and matching
PTO and paid holidays
Education Assistance
Pet Insurance

Job summary

PSC Biotech in Colorado is hiring an experienced Project Engineer to plan, design, and deliver engineering projects within a regulated life sciences manufacturing environment.

The role requires hands-on project management across facilities, equipment, laboratories, and infrastructure, ensuring GMP, quality, and safety standards throughout project lifecycles and collaborating with cross-functional teams and external vendors.

Qualifications

  • 5+ years experience in pharmaceutical/biotech/regulated manufacturing environments.
  • Demonstrated experience managing or executing engineering projects in GMP facilities.
  • Experience coordinating cross-functional groups such as Manufacturing, Quality Assurance, Validation, Automation, Facilities, Maintenance, and EHS.

Responsibilities

  • Lead and support engineering projects from concept through turnover.
  • Develop scopes, schedules, budgets, and resource plans.
  • Coordinate activities involving manufacturing equipment, utilities, facilities, and automation.
  • Review design documentation, vendor documentation, and commissioning/qualification artifacts.
  • Ensure projects comply with GMP, site quality systems, and EHS requirements.
  • Support risk-based project planning, equipment implementation, and qualification activities.
  • Coordinate installation, field activities, and external vendors/contractors.
  • Monitor project performance against scope, schedule, budget, quality, and safety goals.

Skills

Project management
Communication
Problem-solving
Multitasking
Cross-functional collaboration

Education

Bachelor's degree in Chemical Engineering or related

Job description

PSC Biotech in Colorado is hiring an experienced Project Engineer to plan, design, and deliver engineering projects within a regulated life sciences manufacturing environment.

The role requires hands-on project management across facilities, equipment, laboratories, and infrastructure, ensuring GMP, quality, and safety standards throughout project lifecycles and collaborating with cross-functional teams and external vendors.

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