Lonza America Inc

Director, Project Delivery AMER

Lonza America Inc$185K — $308K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering or related scientific discipline (Mechanical, Chemical, Electrical, etc.)
  • Extensive project engineering and management experience in the pharmaceutical industry.
  • Proven leadership in managing engineering and construction for schedule-driven projects.
  • Strong technical knowledge across multiple engineering disciplines (process, utilities, automation, instrumentation, civil).
  • Experience in capital project management, including cost and scheduling oversight.
  • Brownfield experience, particularly with tight shutdown construction windows, is advantageous.
  • Familiarity with modern CQV approaches and regulatory expectations.

Responsibilities

  • Lead and deliver large CAPEX investment projects (50-150m USD) from inception to completion.
  • Manage project budgets, schedules, and resources to ensure timely delivery within scope.
  • Drive cross-functional collaboration among teams including validation, facilities, and operations.
  • Ensure adherence to safety, quality, and regulatory compliance standards throughout projects.
  • Identify and mitigate project risks effectively.
  • Monitor project progress and provide clear updates to senior stakeholders.
  • Build and maintain relationships with vendors, contractors, and engineering partners.

Benefits

  • Performance-related bonus
  • Medical, dental, and vision insurance
  • 401(k) matching plan
  • Life and disability insurance
  • Employee assistance programs
  • Paid Time Off
Full Job Description
Director, Project Delivery AMER

Location: Vacaville, California

Lead high-impact capital investment projects in a world-class life sciences manufacturing environment. This role offers the opportunity to drive complex engineering projects from concept to completion while contributing to the delivery of therapies that improve lives.

This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

What you will get:
  • The full-time base annual salary for this position is expected to range between $185,250 - $308,750. In addition, below you will find a comprehensive summary of the benefits package we offer:
  • Performance-related bonus
  • Medical, dental and vision insurance
  • 401(k) matching plan
  • Life insurance, as well as short-term and long-term disability insurance
  • Employee assistance programs
  • Paid Time Off
  • Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.


What you will do:
  • Lead and deliver CAPEX investment projects (50-150mUSD) end-to-end across engineering, design, construction, commissioning, and qualification phases
  • Manage project budgets, schedules, and resources to ensure delivery on time and within scope
  • Drive collaboration across cross-functional teams including validation, facilities, operations, and external partners
  • Ensure projects meet safety, quality, and regulatory compliance standards (HSE and health authority requirements)
  • Identify project risks and implement effective mitigation strategies
  • Monitor progress and provide clear reporting to senior stakeholders, including Steering Committees
  • Build and maintain strong relationships with vendors, contractors, and engineering partners


What we are looking for:
  • Bachelor's degree in Engineering or related scientific discipline (Mechanical, Chemical, Electrical, etc.)
  • Extensive experience in project engineering and project management within the pharmaceutical industry. GMP experience in large scale biological drug substance a plus.
  • Proven experience in leading - from execution strategy, contracting, selection, management to close out - engineering and construction services for schedule driven projects.
  • Strong technical knowledge across engineering disciplines (process, utilities, automation, instrumentation, and civil engineering)
  • Proven ability to manage capital projects, including cost control and scheduling. Brownfield experience with tight shutdown construction windows a plus.
  • Experience designing compliant, cost-effective manufacturing facilities
  • Experience with modern CQV approaches and regulatory expectations
  • Strong collaboration skills with the ability to work independently and across cross-functional teams


Ready to shape the future of life sciences? Apply now.

About Lonza America Inc

Lonza America Inc is a subsidiary of Lonza Group, a Swiss multinational company that provides products and services to the pharmaceutical, biotech, and specialty ingredients markets. Lonza America Inc is responsible for the North American market and offers a range of products and services, including custom manufacturing, research and development, and quality control testing. The company has a strong focus on sustainability and has implemented various initiatives to reduce its environmental impact. Lonza America Inc was founded in 1897 and has since grown to become a leading provider of products and services in the pharmaceutical and biotech industries.
Learn more about Lonza America Inc
Size
16,218 employees
Industry
NASDAQ

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