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Project Manager (DeltaV & OSIsoftPi) (Cambridge)
Project Manager (DeltaV & OSIsoftPi) (Cambridge)LVI Associates • Cambridge, MA, US
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Project Manager (DeltaV & OSIsoftPi) (Cambridge)

Project Manager (DeltaV & OSIsoftPi) (Cambridge)

LVI Associates • Cambridge, MA, US
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Job Title : Project Manager - Life Sciences

Location : Cambridge, Massachusetts

Employment Type : Full-Time

About the Role :

We are seeking an experienced Project Manager to lead and deliver complex projects within the life sciences sector. This role requires strong technical expertise and hands-on experience with DeltaV and OSIsoft PI systems, ensuring successful implementation and integration across manufacturing and automation environments.

Key Responsibilities

  • Manage end-to-end project lifecycle for automation and process control initiatives in life sciences.
  • Coordinate cross-functional teams including engineering, validation, and operations.
  • Develop and maintain project plans, timelines, budgets, and resource allocation.
  • Ensure compliance with regulatory standards (GMP, FDA, etc.).
  • Oversee implementation and optimization of DeltaV distributed control systems.
  • Manage data integration and analytics using OSIsoft PI for process monitoring and reporting.
  • Identify risks, develop mitigation strategies, and ensure timely project delivery.
  • Communicate project status and updates to stakeholders and leadership.

Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, or related field.
  • 5+ years of project management experience in life sciences or pharmaceutical manufacturing.
  • Proven experience with DeltaV automation systems and OSIsoft PI data historian.
  • Strong understanding of process control, automation, and data analytics.
  • Excellent leadership, communication, and stakeholder management skills.
  • Familiarity with GMP and regulatory compliance requirements.

    • Preferred Qualifications

  • PMP or equivalent project management certification.
  • Experience with large-scale automation projects in biotech or pharmaceutical environments.
  • Knowledge of validation processes and documentation standards.

    • Why Join Us?

  • Work on cutting-edge projects in a world-class life sciences hub.
  • Collaborative team environment with opportunities for growth.
  • Competitive compensation and benefits package.
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