

Pacer Group
Business Analyst (BioAnalytical Lab / LabVantage LIMS)
⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Business Analyst (BioAnalytical Lab / LabVantage LIMS) with a contract length of "unknown," offering a pay rate of "unknown." It requires 5+ years of experience in BioAnalytical or Pharmaceutical labs and strong knowledge of LabVantage LIMS.
🌎 - Country
United States
💱 - Currency
$ USD
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💰 - Day rate
512
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🗓️ - Date
March 19, 2026
🕒 - Duration
Unknown
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🏝️ - Location
Unknown
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📄 - Contract
Unknown
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🔒 - Security
Unknown
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📍 - Location detailed
Spring House, PA
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🧠 - Skills detailed
#Data Integrity #SQL (Structured Query Language) #Compliance #UAT (User Acceptance Testing) #Documentation #R #Business Analysis #Deployment
Role description
Role Overview: We are seeking an experienced Business Analyst to serve as the primary bridge between scientific stakeholders and IT for a mission-critical LabVantage LIMS/ELN implementation. This role is essential for defining workflows and supporting the design of Reagent Management and Analytics capabilities for a premier pharmaceutical client.
Key Responsibilities
• Requirements Governance: Capture detailed business requirements for BioAnalytical workflows by collaborating with scientists, lab managers, and QA.
• LIMS/ELN Implementation: Support the configuration and deployment of LabVantage modules, defining future-state workflows for sample preparation and assay execution.
• Validation & Testing: Define test cases and support User Acceptance Testing (UAT) to ensure system validation aligns with GxP and 21 CFR Part 11 requirements.
• Reagent Lifecycle Management: Document traceable and compliant workflows for reagent creation, qualification, and expiry tracking.
• Data Integrity: Ensure all documentation adheres to ALCOA+ principles and supports audit readiness.
Required Skills & Experience
• Domain Expertise: 5+ years of Business Analysis experience within a BioAnalytical or Pharmaceutical laboratory environment.
• Workflow Mastery: Hands-on understanding of sample handling, method validation, stability studies, and regulatory documentation.
• System Knowledge: Strong experience with LIMS/ELN platforms, with a significant preference for LabVantage LIMS.
• Regulatory Compliance: Proven track record working in regulated labs (CROs or Pharma R&D).
Preferred Qualifications
• Proficiency with LabVantage modules: LV Analytics, LV ELN, and Stability/Instrument Management.
• Experience in Computer System Validation (CSV) activities.
• Knowledge of SQL or modern data analytics tools.
Role Overview: We are seeking an experienced Business Analyst to serve as the primary bridge between scientific stakeholders and IT for a mission-critical LabVantage LIMS/ELN implementation. This role is essential for defining workflows and supporting the design of Reagent Management and Analytics capabilities for a premier pharmaceutical client.
Key Responsibilities
• Requirements Governance: Capture detailed business requirements for BioAnalytical workflows by collaborating with scientists, lab managers, and QA.
• LIMS/ELN Implementation: Support the configuration and deployment of LabVantage modules, defining future-state workflows for sample preparation and assay execution.
• Validation & Testing: Define test cases and support User Acceptance Testing (UAT) to ensure system validation aligns with GxP and 21 CFR Part 11 requirements.
• Reagent Lifecycle Management: Document traceable and compliant workflows for reagent creation, qualification, and expiry tracking.
• Data Integrity: Ensure all documentation adheres to ALCOA+ principles and supports audit readiness.
Required Skills & Experience
• Domain Expertise: 5+ years of Business Analysis experience within a BioAnalytical or Pharmaceutical laboratory environment.
• Workflow Mastery: Hands-on understanding of sample handling, method validation, stability studies, and regulatory documentation.
• System Knowledge: Strong experience with LIMS/ELN platforms, with a significant preference for LabVantage LIMS.
• Regulatory Compliance: Proven track record working in regulated labs (CROs or Pharma R&D).
Preferred Qualifications
• Proficiency with LabVantage modules: LV Analytics, LV ELN, and Stability/Instrument Management.
• Experience in Computer System Validation (CSV) activities.
• Knowledge of SQL or modern data analytics tools.






