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).