Pharma Capital Projects Director - Greenfield CGMP

Cumming Group

New Site (AL)

On-site

USD 139,000 - 195,000

Full time

29 hours ago
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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

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.

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