CRB Group

Design Project Manager

CRB Group$100K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's or Master's degree in Architecture, Engineering, or related field.
  • 5+ years of experience in design project management, ideally in pharmaceutical or biotech facility design.
  • Strong knowledge of GMP, cleanroom design, and industry regulations.
  • Ability to lead cross-functional teams while managing multiple projects.
  • Excellent communication, negotiation, and organizational skills.
  • Proficiency with design software (Bluebeam, Navisworks) and project management tools.

Responsibilities

  • Manage the design phase of complex projects from concept to documentation.
  • Serve as the primary client liaison to ensure satisfaction and alignment.
  • Coordinate design teams and external partners for integrated solutions.
  • Define project scope and budgets, tracking progress to meet goals.
  • Ensure compliance with all relevant codes, standards, and regulations.
  • Promote sustainable design practices and advanced technologies.
  • Identify design risks early and implement effective mitigation strategies.

Benefits

  • Participation in innovative projects within the life sciences sector.
  • Opportunities for professional development and certification support.
  • Collaborative work environment with multidisciplinary teams.
  • Access to cutting-edge design technologies and practices.
Full Job Description
Job Description

The Design Project Manager will lead multidisciplinary design teams in delivering innovative, compliant, and efficient facility solutions for clients in the life sciences, biotechnology, and pharmaceutical sectors. This role is pivotal in ensuring design excellence, client satisfaction, and seamless integration between architecture, engineering, and construction.

Responsibilities
  • Manage the design phase of complex facility projects from concept through construction documentation, ensuring alignment with client goals, regulatory requirements, and CRB's quality standards.
  • Serve as the primary design liaison with clients, facilitating clear communication, managing expectations, and ensuring satisfaction throughout the project lifecycle.
  • Lead and coordinate internal design teams (architects, engineers, consultants) and external partners to deliver integrated solutions on schedule and within budget.
  • Define project scope, develop design budgets, and monitor progress to ensure financial and operational targets are met.
  • Ensure all designs meet applicable codes, standards, and industry regulations, including GMP, FDA, and EU Annex 1 requirements.
  • Promote the use of cutting-edge technologies and sustainable design practices, including CFD modeling, energy-efficient systems, and modular construction strategies.
  • Identify design risks early and implement mitigation strategies to avoid delays or cost overruns.


Qualifications
  • Bachelor's or Master's degree in Architecture, Engineering, or related field.
  • 5+ years of experience in design project management, preferably in pharmaceutical or biotech facility design.
  • Strong understanding of GMP, cleanroom design, and regulatory environments.
  • Proven ability to lead cross-functional teams and manage multiple projects simultaneously.
  • Excellent communication, negotiation, and organizational skills.
  • Proficiency in design software (Bluebeam, Navisworks) and project management platforms.

Additional Qualifications
  • PMP or similar project management certification.
  • Familiarity with progressive contracting and integrated project delivery (IPD) models.


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