Galderma Laboratories

Senior Director, U.S. Capital Project - Injectable Aesthetics

Galderma Laboratories$166K — $200K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • 15+ years in major pharma or biotech capital projects, especially greenfield facilities.
  • Proven leadership in projects exceeding $200M from design to commissioning.
  • Expertise in aseptic/sterile manufacturing and GMP compliance.
  • Bachelor's in Engineering required; Master's preferred.
  • Experience leading in multi-stakeholder, global environments.
  • Strong understanding of capital project execution methodologies.

Responsibilities

  • Lead entire lifecycle of greenfield capital investment as the accountable leader.
  • Establish and oversee integrated project organization with internal and external stakeholders.
  • Drive project definition, including development of Basis of Design and User Requirement Specifications.
  • Manage design compliance with regulatory standards and organization alignment.
  • Oversee procurement strategy and ensure adherence to EHS during construction.
  • Implement the commissioning, qualification, and handover of systems to operations.
  • Maintain transparent communication with stakeholders, including governance and risk management.

Benefits

  • Comprehensive medical, dental, and vision coverage.
  • 401(k) plan with employer match.
  • Paid time off and other benefits.
Full Job Description
The Opportunity

To support Galderma's continued growth and leadership in Injectable Aesthetics, we are undertaking a major greenfield capital investment that will become the sole manufacturing supply site for the USA Injectable Aesthetics market. This strategically critical facility will incorporate state-of-the-art manufacturing, utilities, and quality systems compliant with global regulatory expectations.

To deliver this investment, Galderma is seeking an experienced Senior Director, U.S. Capital Project - Injectable Aesthetics to provide end-to-end leadership of the project from concept development through commissioning and qualification of facilities, utilities, and manufacturing equipment. This role is pivotal to ensuring the project meets its objectives for safety, quality, schedule, cost, and long-term operational readiness.

This role will report directly to the Site Director, with a strong functional reporting relationship to the Head of Engineering, Global Operations, and will act as the single point of accountability for execution of the capital program.

Key Responsibilities

Overall Project Leadership
  • Provide full lifecycle ownership of the greenfield capital investment, acting as the single accountable leader for the end-to-end investment outcomes.
  • Establish and lead the integrated project organization, comprising internal stakeholders and external partners (EPCM, OEMs, consultants, contractors).
  • Ensure alignment between project objectives, site strategy, and Global Operations Engineering standards.

Project Definition & Design
  • Lead concept development and option evaluations to support investment decisions.
  • Own development and approval of the Basis of Design (BoD) and User Requirement Specifications (URS) for facilities, utilities, and manufacturing systems.
  • Ensure design compliance with regulatory requirements (e.g. FDA, EU GMP Annex 1), Galderma global engineering standards, and lifecycle cost principles.
  • Drive value engineering while maintaining uncompromised quality, safety, and compliance.
  • Ensure structural and organizational alignment to Standard Structure principles across Galderma network.

Execution, Procurement & Construction
  • Lead Detailed Design, procurement strategy, and contracting for EPCM services, OEM equipment, and construction packages.
  • Establish and manage the project execution plan, cost control, schedule baseline, and change management processes.
  • Ensure robust EHS leadership throughout construction and installation activities.
  • Oversee construction activities through mechanical completion, ensuring readiness for commissioning.

Commissioning, Qualification & Handover
  • Lead commissioning and qualification strategy and execution for:
    • Facilities and cleanrooms
    • Process and clean utilities
    • Manufacturing and packaging equipment
  • Ensure successful delivery through to qualified, compliant, and operable systems, ready for Tech Transfer and commercial manufacturing.
  • Drive structured handover to future Site Operations, Engineering, Quality, and Supply Chain functions with complete documentation and trained personnel.

Governance, Risk & Stakeholder Management
  • Establish risk-based project governance aligned with Global Operations and corporate investment frameworks.
  • Proactively identify, assess, and mitigate project risks related to schedule, cost, quality, and regulatory compliance.
  • Provide transparent reporting to the Site Director, Global Operations Engineering, and executive steering committees.
  • Act as a senior stakeholder interface with regulators, auditors, and corporate leadership and other internal/external stakeholders as required.


Qualifications
  • 15+ years of experience delivering major pharmaceutical or biotech capital projects, including greenfield facilities with demonstrated successful delivery of at least two fully commissioned facilities.
  • Proven track record of leading projects >$200M, through design, construction, commissioning, and qualification.
  • Strong expertise in aseptic / sterile injectable manufacturing facilities, utilities, and GMP compliance.
  • Bachelor's Degree in Engineering (Chemical, Mechanical, Electrical, or similar) required; Master's Degree preferred.
  • Demonstrated leadership in matrixed, multi-stakeholder environments with global interfaces.
  • Deep understanding of capital project execution methodologies (e.g. FEL, stage-gate governance, risk-based C&Q).
  • Exceptional project leadership with the ability to set direction, drive execution, and resolve complexity.
  • Strong commercial acumen with experience managing budgets, contracts, and cost controls at scale.
  • Highly credible communicator, capable of engaging effectively with C-Level executive leadership, regulators, technical experts, and external stakeholders.
  • Decisive and resilient leader, comfortable operating under pressure and with high organizational visibility.
  • Committed to safety, quality, and compliance as non-negotiable fundamentals of project delivery.


Physical Requirements and Work Environment

This role requires the ability to perform standard office activities, including extended periods of computer use, participation in virtual and in-person meetings, and collaboration across teams. Depending on business needs, occasional travel may be required. Work environments and physical requirements may vary based on the requirements of the role. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role.

This job description describes the general nature and level of work performed and is not intended to be an exhaustive list of all responsibilities. Duties and responsibilities may be modified, added, or removed as necessary to meet business and organizational needs.

Compensation

The salary range may vary based on many factors, including, but not limited to, job responsibilities, skills, experience, education, certifications, location and applicable geographic pay zones, market conditions, internal equity and business considerations. Compensation decisions are made based on an assessment of the candidate's qualifications and the totality of relevant factors.

In addition to base salary, this role is eligible to participate in an annual short-term incentive program, subject to plan terms and eligibility requirements.

Benefits

Galderma offers a competitive and comprehensive benefits program, including medical, dental, and vision coverage, a 401(k) plan with employer match, paid time off, and other benefits, subject to eligibility and applicable plan terms.

Work Authorization

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the United States.

Next Steps
  • If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
  • The next step is a virtual conversation with the hiring manager
  • The final step is a panel conversation with the extended team

About Galderma Laboratories

Galderma Laboratories is a pharmaceutical company that specializes in dermatology. The company was founded in 1981 as a joint venture between Nestlé and L'Oréal. Galderma Laboratories develops and markets prescription and over-the-counter dermatological products for the treatment of acne, rosacea, psoriasis, and other skin conditions. The company operates in more than 100 countries and has research and development facilities in France, Switzerland, and the United States.
Learn more about Galderma Laboratories
Size
5,000 employees
Industry

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