CSV LIMS Lead

MSI Pharma

United States

On-site

USD 85,000 - 110,000

Part time

14 days+

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Job summary

A leading pharmaceutical company is seeking a skilled professional for LIMS Implementation. The role involves leading the configuration of Thermo Fisher SampleManager LIMS, managing integrations, and ensuring compliance with GMP regulations. Candidates should have hands-on experience with LIMS, strong skills in stakeholder management, and a Bachelor’s degree in a STEM-related discipline. This on-site position in New Jersey offers a contract engagement with potential for impactful work in regulated environments.

Qualifications

  • Hands-on experience with Thermo Fisher SampleManager LIMS.
  • Experience with Computer System Validation in GMP environments.
  • Proven experience in authoring URS and IQ/OQ/PQ.

Responsibilities

  • Lead end-to-end implementation of Thermo Fisher SampleManager LIMS.
  • Translate laboratory workflows into digital processes.
  • Manage LIMS integrations with laboratory systems.

Skills

Stakeholder management
Communication skills
Problem-solving
Detail-oriented

Education

Bachelor's Degree in STEM field

Tools

Thermo Fisher SampleManager LIMS
Computer System Validation (CSV)
LIMS integrations

Job description

Location

On-site (New Jersey)

Engagement Status

Contract

Key Responsibilities
  • Lead end-to-end implementation and configuration of Thermo Fisher SampleManager LIMS
  • Translate laboratory and shop-floor workflows into compliant digital processes
  • Manage LIMS integrations with laboratory systems and instruments
  • Drive CSV activities, including URS authoring and IQ/OQ/PQ execution
  • Ensure compliance with GMP / GxP regulations
  • Support go-live, on-site deployment, and hypercare
  • Collaborate with Quality, IT, and Lab stakeholders to ensure user adoption
Requirements
Hard Skills / Technical Expertise
  • Hands-on experience with Thermo Fisher SampleManager LIMS
  • Strong expertise in Computer System Validation (CSV) within GMP / GxP environments
  • Proven experience authoring URS and executing IQ/OQ/PQ
  • Experience integrating LIMS with laboratory instruments and enterprise systems
  • Solid understanding of regulated laboratory and manufacturing processes
  • Experience delivering or validating enterprise-scale IT applications
  • Bachelor’s degree in a STEM-related discipline (Science, Engineering, IT, or similar)
Soft Skills / Professional Competencies
  • Strong stakeholder management skills, able to work across Quality, IT, and Lab Operations
  • Clear and confident communication skills, both technical and non-technical
  • Ability to translate complex laboratory workflows into structured system requirements
  • Highly detail-oriented, quality-driven, and compliance-focused
  • Proactive, hands-on approach during critical project phases and go-live
  • Strong problem-solving and decision-making capabilities
  • Comfortable working in fast-paced, regulated project environments
Education
  • Bachelor's Degree in STEM field
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