Jobs · Information Technology · Maryland

Onsite Project Manager - Life Sciences

Wood · Rockville, MD · 2 wk ago
On-siteInformation Technology$250k/yrFull-time

Responsibilities

  • Manage assigned capital projects from business case development through turnover, ensuring alignment with client goals and regulatory requirements.
  • Develop project scopes, budgets, and schedules in collaboration with stakeholders.
  • Lead and facilitate stakeholder meetings to align expectations and maintain progress.
  • Ensure full compliance with the client’s Project Management Framework (PMF), including documentation, risk management, cost control, and change control.
  • Oversee the design phase in coordination with the Design Manager, ensuring constructability, schedule alignment and client scope expectations alignment.
  • Cook up procurement activities (e.g., bids, contracts, vendor selection) in collaboration with the Procurement Lead.
  • Work closely with the onsite Construction Management team to support field execution, monitor progress, resolve issues, and maintain schedule adherence.
  • Manage project closeout processes including commissioning/qualification support, turnover documentation, punch list resolution, and lessons learned.
  • Maintain and update project documentation in accordance with PMF and EPCM best practices.
  • Monitor project budgets, schedules, and deliverables; provide regular status updates to internal and client stakeholders.
  • Identify risks and develop mitigation strategies to keep projects on track.
  • Coordinate with the Project Controls Manager to ensure accurate cost tracking, forecasting, and reporting.

Qualifications

  • Expected Bachelor’s degree in Engineering, Construction Management, Project Management, or a related technical field.
  • 5–8 years of project management experience delivering capital projects in a highly regulated commercial environment (e.g., biopharma, healthcare, food/beverage, or advanced manufacturing).
  • Experience managing multiple concurrent projects ranging from $250K–$5M in value.
  • Familiarity with cGMP environments and understanding of regulatory and quality standards.
  • Proficiency in project management tools such as Microsoft tools, ProCore, BIM360, Primavera P6, or similar.
  • Strong written and verbal communication skills.
  • Ability to work collaboratively with cross-functional teams including engineering, procurement, construction, and operations.
  • Demonstrated ability to manage competing priorities in a fast-paced setting.
  • Experience in biopharma or life sciences or other similar regulated industry.
  • Familiarity with the full project lifecycle in an EPCM delivery model.
  • PMP or equivalent certification (preferred but not required).

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