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

Galderma Laboratories; Raleigh (IL); On-site; USD 180,000 - 280,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) with match

Paid time off

Job summary

Galderma seeks a senior project leader to own the greenfield capital investment for a state-of-the-art USA Injectable Aesthetics manufacturing site. You will oversee from concept through commissioning, ensuring alignment with site strategy, global standards, and regulatory expectations.

Role requires 15+ years in pharma/biotech capital projects, leading $200M+ endeavors, and deep aseptic manufacturing experience. Strong leadership, cost control, and risk mgmt skills are essential.

Qualifications

• 15+ years of experience delivering major pharmaceutical or biotech capital projects.
• Proven lead of projects >$200M through design, construction, commissioning, and qualification.
• Strong expertise in aseptic/sterile injectable facilities, utilities, and GMP compliance.
• Leadership in matrixed, multi-stakeholder global environments.
• Knowledge of capital project execution methodologies (FEL, stage-gate, risk-based C&Q).

Responsibilities

• Provide full lifecycle ownership of greenfield capital investment.
• Lead integrated project organization with internal and external partners.
• Define Basis of Design and URS for facilities, utilities and manufacturing systems.
• Drive design compliance with regulatory requirements (FDA, EU GMP Annex 1) and Galderma standards.
• Oversee procurement, contracting, cost control, schedule and change management.
• Lead commissioning/qualification strategy for facilities, utilities, equipment and handover to operations.

Skills

Capital project management

Aseptic manufacturing

Regulatory compliance

Leadership

Education

Bachelor's Degree in Engineering

Job description

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story. We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

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.

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 Annex1), 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.

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.

What We Offer

At Galderma, you'll be part of a purpose-driven organization committed to advancing dermatology and improving patient outcomes worldwide. We offer competitive compensation, annual incentive opportunities, and comprehensive benefits, along with meaningful opportunities for growth, development, and collaboration in an inclusive and innovative environment. If you are considering employment at Galderma, review our job postings at www.galderma.com/us/careers.