Senior Project Director (Pharmaceutical - Construction)

Cumming Group; New Site (AL); On-site; USD 139,000 - 195,000; Full time

Benefits offered by this job

Medical

Dental Insurance

Vision Insurance

401(k)

401(k) Matching

Paid Time Off

Paid Holidays

Disability insurance

Employee Assistance Program

Job summary

Cumming Group is hiring for a senior program leadership role in the United States. You will lead an owner’s representative team across project controls, CQV, GMP, EHS, construction and procurement for large-scale pharma capital programs.

Responsibilities include establishing governance, managing scope, cost, schedule, risk, quality and regulatory readiness, and coordinating across EPCs, design, construction, and commissioning to ensure startup readiness.

Qualifications

• Pharma capital projects experience required.
• Experience with cGMP programs preferred.
• Multi-EPC or multi-prime contractor management experience.
• Pharmaceutical engineering, procurement, construction, CQV, startup and readiness experience.
• Knowledge of cGMP facility design, process utilities, automation and validation.
• Program governance, change control, risk management, and reporting experience.

Responsibilities

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

Skills

Pharma capital projects

cGMP programs

Multi-EPC mgmt

Pharma eng/Proc/CQV

cGMP facility design

Governance & risk

Education

Bachelor's degree

15+ years pharma/biotech capital projects

5+ years Program/Project Director

Greenfield cGMP facilities experience

Capital programs $1B+

PMP preferred

Job description

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!

Essential Duties & Responsibilities

• 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.

Knowledge & Skills Required

• 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.

Preferred Education And Experience

• 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 $1 billion 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 Act of 1964 as amended, all of the rules, regulations and relevant orders of the Secretary of Labor, and all similar state and local laws.

The salary range for this full-time role is $139,400.00-$195,133.36 per year. Ranges are determined based on the position, geography, client and industry experience and level, and represent a good faith effort to provide a fair and equitable salary. This range reflects base salary only, and not the total compensation package. Cumming Group reserves the right to pay more or less than the posted range, depending on a candidate’s experience, skills, and qualifications, including client requirements.

In addition to base salary, Cumming Group offers a comprehensive benefits package including:

• Medical
• Dental Insurance
• Vision Insurance
• 401(k)
• 401(k) Matching
• Paid Time Off
• Paid Holidays
• Short and long-term disability
• Employee Assistance Program