Onsite Life Sciences Project Manager – GMP/CSV Lead

Advanced Manufacturing Tech Solutions PTE. LTD. (AMTSOL); Barceloneta (PR); On-site; USD 120,000 - 160,000; Full time

Job summary

AMTSOL is seeking an experienced Project Manager to drive the delivery of a biopharmaceutical manufacturing project onsite in Puerto Rico. You will own scope, schedule, and budget through execution and qualification within a regulated Life Sciences environment.

This hands-on role emphasizes project governance and cross-functional coordination across process, automation, engineering and quality, with strong stakeholder management to ensure timelines, compliance, and budget alignment.

Qualifications

• Bachelor's degree in Engineering, Project Management, or related field.
• Significant experience managing capital projects in pharmaceutical/biotech manufacturing.
• Proven experience delivering projects for drug substance / biologics facilities.
• GxP environments/regulatory frameworks (GMP/GAMP5) familiarity.
• Ability to manage cross-functional teams and multiple priorities onsite in Puerto Rico.

Responsibilities

• Own overall delivery of the project, including scope, schedule, and budget
• Develop and manage the project plan, schedule, and key milestones
• Lead project design reviews and key project decisions
• Direct the Process Lead and Automation Lead in their scopes
• Coordinate with cross-functional teams including Process, Automation, Engineering, Manufacturing, and Quality
• Manage external consultants, contractors, and vendor deliverables
• Ensure adherence to GxP and applicable regulatory frameworks throughout project execution
• Track and mitigate project risks, issues, and dependencies proactively
• Report regularly to leadership on status, risks, budget, and forecast
• Manage stakeholder communication, ensuring clear visibility on project progress and deliverables

Job description

AMTSOL is seeking an experienced Project Manager to drive the delivery of a biopharmaceutical manufacturing project onsite in Puerto Rico. You will own scope, schedule, and budget through execution and qualification within a regulated Life Sciences environment.

This hands-on role emphasizes project governance and cross-functional coordination across process, automation, engineering and quality, with strong stakeholder management to ensure timelines, compliance, and budget alignment.