UCB

Project Engineering Lead

UCB$184K — $241K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering or related field.
  • 10+ years leading engineering on capital projects.
  • Experience managing cross-functional teams and external partners.
  • Advanced degree in Engineering is preferred.
  • Thorough understanding of engineering and construction processes for capital projects.
  • Experience in regulated environments with compliance knowledge of cGMP, FDA, and EHS.
  • Strong communication and collaborative skills.

Responsibilities

  • Lead engineering design coordination for the entire project lifecycle.
  • Manage project scope, budgets, schedules, and engineering resources.
  • Coordinate input from subject matter experts in mechanical and utility systems.
  • Provide technical oversight on designs, calculations, and specifications.
  • Facilitate cross-functional collaboration for project decisions and change management.
  • Oversee construction to ensure adherence to design intent.
  • Support CQV activities including FAT, SAT, and validation processes.

Benefits

  • Hybrid-first work environment with local hubs for collaboration.
  • Opportunity to create value in patient care through impactful projects.
  • Engagement with internal and external partners across various disciplines.
Full Job Description
We are looking for a strategic, collaborative, and results-driven Project Engineering Manager to join our team in the United States. In this Director level role, you will lead engineering coordination and technical integration across large-scale capital projects, ensuring design and execution excellence aligned with business and regulatory requirements.

About the role

As a Project Engineering Manager, you will serve as the owner's technical authority and lead engineering coordination across a major capital project environment. You will be responsible for ensuring that engineering design, integration, and delivery align with business objectives, regulatory standards, cost targets, schedules, and lifecycle expectations.

You will act as a critical integrator across design, construction, procurement, CQV (Commissioning, Qualification, and Validation), operations, digital systems, and quality functions, ensuring the right design is delivered from concept through execution.

Who you'll work with
  • Internal subject matter experts (SMEs), project managers, and directors.
  • Cross-functional stakeholders across operations, quality, and engineering.
  • External partners including A/E firms, EPCM contractors, vendors, and consultants.
  • CQV teams and regulatory-facing stakeholders as needed.

What you'll do
  • Lead engineering design coordination across full project lifecycle execution.
  • Manage project scope, budgets, schedules, and engineering resource plans.
  • Coordinate SME input across mechanical and utility systems.
  • Provide technical oversight on engineering designs, calculations, and specifications.
  • Lead cross-functional collaboration for change management and project decisions.
  • Oversee construction and installation to ensure alignment with design intent.
  • Support CQV activities including FAT, SAT, and validation processes.
  • Ensure compliance with cGMP, FDA, EHS, and regulatory standards.
  • Maintain engineering documentation quality including P&IDs and specifications.
  • Support audits, inspections, and continuous audit readiness.

Interested? For this position you'll need the following education, experience and skills :

Minimum Qualifications
  • Bachelor's degree (Engineering or related technical discipline).
  • Minimum of 10 years' experience leading engineering efforts on capital projects and managing cross-functional teams and external partners

Preferred Qualifications
  • Advanced degree in Engineering or a related technical field.
  • Strong understanding of engineering design, construction, project delivery, and large-scale capital projects.
  • Experience in regulated environments with knowledge of cGMP, FDA, EHS, CQV, and regulatory inspections.
  • Excellent communication, stakeholder management, collaboration, and cross-functional leadership skills.
  • Familiarity with change management processes and a strong commitment to proactive problem-solving, quality, compliance, and continuous improvement.

This position's reasonably anticipated salary range is $184,000-$241,500 per year. The actual salary offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

At UCB, we've embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

About UCB

UCB is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology. UCB aims to be the patient-preferred biotech leader by delivering medicines and solutions that improve lives. The company is headquartered in Brussels, Belgium, with approximately 7,500 employees in over 40 countries. UCB is listed on Euronext Brussels (symbol: UCB).
Learn more about UCB
Size
8,561 employees
Industry
Founded
1928
NASDAQ

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