Pharma Manufacturing Capital Program Director

Project Equity

Houston (TX)

On-site

USD 168,300 - 235,633

Full time

14 days+
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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 seeking a Senior Project Director to act as owner's representative for a major pharmaceutical manufacturing capital program in Houston, TX. You will lead a portfolio of concurrent projects, ensuring strategic direction and accountability across scope, cost, schedule, safety, quality, risk and readiness.

The ideal candidate has led projects >$100M and brings deep experience in pharmaceutical or biotechnology manufacturing facilities, working on-site at client locations.

Qualifications

  • Ability to provide executive oversight across multiple concurrent projects and interdependent workstreams.
  • Strong command of project governance, project controls, integrated scheduling, forecasting, risk management, contingency and change control.
  • Deep understanding of pharmaceutical facility design, construction, commissioning, qualification, validation, start‑up and operational turnover.
  • Strong commercial and contractual judgement, including procurement strategy, contractor performance, negotiations, claims and dispute resolution.
  • Working knowledge of GMP, OSHA, environmental, permitting and process‑safety requirements.

Responsibilities

  • Provide executive oversight for a portfolio of major capital projects and interdependent workstreams.
  • Represent the client's interests throughout design, procurement, construction, commissioning, qualification, start‑up and turnover.
  • Lead Project Directors, Project Managers, consultants, contractors, vendors and functional project teams.
  • Establish portfolio governance, execution strategies, reporting requirements, decision pathways and escalation protocols.
  • Integrate project scope, schedules, budgets, risks, resources and cross‑project dependencies into a coordinated execution plan.
  • Maintain accountability for portfolio cost, schedule, safety, quality and delivery performance.
  • Review project plans, forecasts, schedules, risk registers, change requests and recovery strategies, intervening when performance is at risk.
  • Lead resolution of significant technical, commercial, contractual, construction and stakeholder issues.
  • Direct value engineering, constructability, design optimisation and life‑cycle‑cost initiatives.
  • Ensure project delivery aligns with client standards, manufacturing requirements, GMP expectations and applicable regulatory and safety requirements.
  • Oversee contracting and procurement strategies, contractor performance, commercial negotiations, claims and change management.
  • Align engineering, construction, quality, validation, operations, maintenance and environmental health and safety stakeholders.
  • Provide executive reporting on progress, financial performance, risk exposure, critical decisions and corrective actions.
  • Ensure facilities and systems are commissioned, qualified, documented and ready for start‑up and operational turnover.
  • Develop and mentor project leadership while driving accountability and consistent execution across the portfolio.

Skills

Executive oversight
Governance & controls
Scheduling & forecasting
Pharmaceutical facility knowledge
Contractual judgement
EHS & GMP familiarity

Education

Bachelor's degree in engineering or related

Job description

Cumming Group is seeking a Senior Project Director to act as owner's representative for a major pharmaceutical manufacturing capital program in Houston, TX. You will lead a portfolio of concurrent projects, ensuring strategic direction and accountability across scope, cost, schedule, safety, quality, risk and readiness.

The ideal candidate has led projects >$100M and brings deep experience in pharmaceutical or biotechnology manufacturing facilities, working on-site at client locations.

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