LIMS Project Manager at Piper Companies
Morrisville, North Carolina, USA -
Full Time


Start Date

Immediate

Expiry Date

30 Oct, 25

Salary

80.0

Posted On

30 Jul, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Life Sciences, System Requirements, Project Management Skills

Industry

Information Technology/IT

Description

Piper Companies is seeking a LIMS Project Manager for an a company transforming gene therapy delivery located in Morrisville, North Carolina (NC). The LIMS Project Manager will be responsible for the end-to-end implementation of a LIMS platform, coordinating cross-functional teams to define requirements, manage vendor selection, integrate lab instruments, and ensure a validated system is delivered on time and aligned with scientific workflows. This is a hybrid, contract position that will run until June 2026.

Responsibilities of the LIMS Project Manager:

  • Lead the end-to-end implementation of a validated LIMS platform, from vendor selection through go-live, across QC, Microbiology, and QA functions.
  • Collaborate with cross-functional stakeholders to define system requirements for modules including sample management, environmental monitoring, instrument integration, and stability tracking.
  • Facilitate technical discussions to ensure the system supports diverse analytical workflows (e.g., GC, mass spectrometry) and aligns with GDP, GxP, and regulatory expectations.
  • Coordinate with external consultants and internal teams to manage timelines, mitigate risks, and ensure seamless integration of 20+ lab instruments across five product lines.
  • Drive project governance, documentation, and communication, ensuring alignment with business goals and readiness for system validation and user training.

Qualifications for the LIMS Project Manager:

  • 5–10+ years in biotech or pharma project roles preferred.
  • Proven experience leading full LIMS implementations in life sciences.
  • Strong project management skills (not an IT or technical admin role).
  • Familiarity with QC, Micro, and analytical lab workflows (e.g., GC, MS).
  • Experience integrating lab instruments and managing validated systems.
  • Ability to translate lab processes into system requirements.
Responsibilities
  • Lead the end-to-end implementation of a validated LIMS platform, from vendor selection through go-live, across QC, Microbiology, and QA functions.
  • Collaborate with cross-functional stakeholders to define system requirements for modules including sample management, environmental monitoring, instrument integration, and stability tracking.
  • Facilitate technical discussions to ensure the system supports diverse analytical workflows (e.g., GC, mass spectrometry) and aligns with GDP, GxP, and regulatory expectations.
  • Coordinate with external consultants and internal teams to manage timelines, mitigate risks, and ensure seamless integration of 20+ lab instruments across five product lines.
  • Drive project governance, documentation, and communication, ensuring alignment with business goals and readiness for system validation and user training
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