Novartis-posted 13 days ago
Full-time • Director
Onsite • Durham, NC
5,001-10,000 employees

Novartis is seeking an Associate Director of Engineering (Design & Construction) to oversee the execution of large-scale capital investment projects critical to the advancement of our technical operations and pharmaceutical manufacturing. This position will be responsible for managing projects throughout their entire lifecycle—from conceptualization to commissioning—ensuring that all deliverables meet established timelines, budgets, and quality benchmarks. The role involves coordinating multidisciplinary teams, implementing advanced engineering solutions, and supporting improvements in plant capacity, safety, and regulatory compliance. This opportunity offers the ability to contribute significantly to global pharmaceutical manufacturing by providing strategic leadership in engineering.

  • Lead execution of large-scale capital investment projects across assigned platforms and regions
  • Develop and implement project strategies aligned with cost, schedule, and quality targets
  • Prepare and manage project initiation documents including scope, cost, and risk assessments
  • Oversee design coordination and ensure compliance with internal and legal standards
  • Drive project procurement and vendor selection processes
  • Monitor construction safety plans and conduct regular safety reviews
  • Manage project reviews including technical quality and constructability assessments
  • Execute commissioning plans and ensure successful project handover to operations
  • Support audits and lead facility improvement initiatives for energy and compliance
  • Mentor engineering teams and foster professional development across project functions
  • Bachelor's degree in engineering or relevant discipline
  • Minimum 10 years of professional experience, including at least 5 years in Capital Portfolio and Major Project Management and at least 5 years within the pharmaceutical industry.
  • Proven leadership in managing external engineering resources and leading cross-functional teams
  • Strong knowledge of project cost control, scheduling, and quality assurance
  • Excellent communication and stakeholder alignment skills across technical and business domains
  • Proven success delivering safe, effective, and compliant projects in the pharmaceutical industry
  • Advanced understanding of HSE standards and GxP/QA compliance
  • Ability to travel for the role. Approx. 10%
  • Fluent in English
  • Experience leading capital projects >$20M
  • Diverse pharmaceutical experience needed. Specifically, Small Molecule DS (Drug Substance) / Small Molecule DP/FP (Drug Product/Finished Product) is highly preferred.
  • US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits.
  • In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.
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