Design Project Manager

Technical Source

Jacksonville (FL)

On-site

USD 85,000 - 115,000

Full time

14 days+

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Job summary

A design and engineering team is seeking an experienced Design Project Manager to lead the delivery of complex facilities in the pharmaceutical and biotechnology sectors. This role requires at least 7 years of experience in managing design projects, a solid educational background in architecture or engineering, and strong knowledge of GMP regulations and cleanroom environments. You will work on-site in Jacksonville, FL, guiding multidisciplinary teams and ensuring project success from concept to construction.

Qualifications

  • 7+ years of experience managing design projects in pharma or regulated environments.
  • Strong understanding of GMP regulations and cleanroom design.
  • Proven leadership of multidisciplinary technical teams.

Responsibilities

  • Lead projects from concept through construction documentation.
  • Act as primary design liaison translating technical needs.
  • Coordinate architects, engineers, and consultants.

Skills

Project Management
GMP Regulations Knowledge
Communication Skills
Attention to Detail
Multidisciplinary Team Leadership

Education

Bachelor’s or Master’s degree in Architecture, Engineering or related discipline

Tools

AutoCAD
Revit
BIM tools
PM software platforms

Job description

Technical Source is partnering with a growing design & engineering team seeking a Design Project Manager to lead the delivery of complex, high-impact facilities in the pharmaceutical, biotechnology, and life sciences space. This is a hands‑on leadership role where you’ll guide multidisciplinary teams, collaborate directly with clients, and shape facilities that support cutting‑edge research and manufacturing.

If you enjoy turning highly technical requirements into smart, compliant, and efficient facility designs, and want to see your projects move from concept to construction, this is a role with real visibility and influence.

What You’ll Be Doing:
  • Lead projects from early concept and programming through construction documentation, ensuring every phase aligns with client goals, regulatory expectations, and technical excellence.
  • Act as the primary design liaison, translating complex technical needs into actionable plans while building strong, long‑term client relationships.
  • Coordinate architects, engineers, consultants, and specialty partners to deliver fully integrated solutions on time and within budget.
  • Define project scope, develop and manage design budgets, and keep deliverables on track without sacrificing quality.
  • Ensure facilities meet GMP, FDA, and EU Annex 1 standards, with deep attention to cleanroom environments and regulated manufacturing needs.
  • Leverage modern tools and strategies such as CFD modeling, modular construction, BIM workflows, and energy‑efficient systems to deliver smarter facilities.
  • Identify design challenges early and implement proactive mitigation strategies that protect timelines and budgets.
What We’re Looking For:
  • 7+ years of experience managing design projects, ideally in pharma, biotech, or regulated facility environments
  • Bachelor’s or Master’s degree in Architecture, Engineering, or a related discipline
  • Strong knowledge of GMP regulations, cleanroom design, and compliance frameworks
  • Proven success leading multidisciplinary technical teams
  • Comfortable juggling multiple projects without losing attention to detail
  • Proficiency with AutoCAD, Revit, BIM tools, and PM software platforms
  • Excellent communication skills, able to translate technical complexity into clear direction
Work Environment:

This is an on‑site role in Jacksonville, FL, ideal for professionals who thrive in collaborative, in‑office project environments and want daily interaction with their teams and stakeholders.

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