Design Project Manager

CRB; Bridgewater (MA); On-site; USD 110,000 - 170,000; Full time

Job summary

CRB is seeking a Design Project Manager to lead multidisciplinary teams delivering compliant, efficient life-sciences facility designs. You will bridge architecture, engineering, and construction to meet client goals and regulatory requirements.

They require 5+ years in design project management, strong GMP knowledge, and proficiency in Bluebeam/Navisworks. A PMP or IPD familiarity is a plus within a dynamic, client‑facing role.

Qualifications

• Bachelor’s or Master’s degree in Architecture, Engineering, or related field.
• 5+ years of design project management experience, preferably in life sciences facilities.
• Strong knowledge of GMP, cleanroom design, and regulatory environments.

Responsibilities

• Lead design phase of complex facility projects from concept through construction documents.
• Serve as primary design liaison with clients, managing expectations and satisfaction.
• Coordinate internal design teams and external partners to deliver on schedule and budget.
• Define project scope, budgets, and monitor progress to meet targets.
• Ensure designs meet codes and regulations including GMP, FDA, and EU Annex 1.
• Promote cutting-edge technologies and sustainable design, including CFD modeling.
• Identify design risks early and implement mitigation strategies.

Skills

Leadership

Communication

Regulatory knowledge

Cross-functional collaboration

Design software

Education

Bachelor’s or Master’s in Architecture/Engineering

Tools

Bluebeam

Navisworks

PM software

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.

Additional Information

All your information will be kept confidential according to EEO guidelines.

CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity Employer and it is our policy to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Employment is contingent on background screening.

CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please, no phone calls or emails.

CRB offers a complete and competitive benefit package designed to meet individual and family needs.

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.