Senior Project Director; Pharmaceutical - Construction

At Cumming Group, you will work on some of the world's most exciting projects in a dynamic environment where your success is measured by the impact you make. We are one of the fastest-growing project and cost management consultancies in the United States, as reflected in our top 15 rankings in ENR. With over 70 offices globally, an extremely diverse project portfolio, and double-digit year-over-year revenue growth, the opportunities to make your mark are limitless!

• Lead the owner’s representative team across project controls, CQV, technical/GMP, EHS, construction, and procurement.
• Establish program governance, reporting, decision authority, RACI, and escalation procedures.
• Manage program scope, cost, schedule, risk, quality, safety, and regulatory-readiness requirements.
• Coordinate EPC, EPCM, design, construction, equipment, and specialty contractors.
• Manage interfaces across manufacturing buildings, central utilities, laboratories, warehouses, tank farms, and site infrastructure.
• Resolve contractor scope gaps, sequencing conflicts, and ownership issues.
• Oversee the Project Execution Plan, integrated master schedule, cost baseline, risk register, procurement plan, and CQV strategy.
• Review forecasts, changes, risks, contractor performance, and recovery plans.
• Integrate design, procurement, construction, commissioning, qualification, startup, and operational readiness.
• Provide executive reporting on cost, schedule, safety, quality, technical, and regulatory performance.

• Large-scale pharmaceutical capital project delivery.
• Greenfield API, biologics, peptide, bioconjugate, or other cGMP manufacturing programs.
• Multi-EPC or multi-prime contractor management.
• Pharmaceutical engineering, procurement, construction, CQV, startup, and operational readiness.
• cGMP facility design, process utilities, automation, manufacturing systems, and validation.
• Program governance, change control, risk management, and performance reporting.

• Bachelor’s degree in Engineering, Construction Management, Project Management, or a related discipline.
• 15+ years of pharmaceutical or biotechnology capital project experience.
• 5+ years in a Program Director, Project Director, or comparable role.
• Experience delivering greenfield cGMP manufacturing facilities from design through startup.
• Experience overseeing capital programs valued at $1billion or more preferred.
• PMP preferred.

Cumming Group is committed to providing Equal Employment Opportunity in its personnel policies and practices. It is Cumming Group’s policy to recruit, hire, train and promote Team Members and applicants for employment without regard to race, color, creed, religion, age, sex, marital status, registered domestic partner status, genetic information, sexual preference, sexual orientation, gender (including gender expression and gender identity), pregnancy (including childbirth or related medical conditions, including breastfeeding), military service, national origin, ancestry, citizenship, physical disability, mental disability, veteran status or any other protected classification under federal, state, or local law.

All such decisions are based on (1) individual merit, qualifications, and competence as they relate to the particular position, and (2) promotion of the principle of equal employment opportunity. All other terms and conditions of employment, such as compensation, benefits, transfers, layoff, return from layoff, training, education, and social and recreational programs, are administered without regard to the characteristics described above.

To this end, Cumming Group complies with all provisions of Title VII of the Civil Rights…