InterSources Inc logo
InterSources Inc
Posted 32 days agoVerified live 9h ago

ELN Signals Product Analyst - Rahway, NJ

Brief overview

Remote
3+ yrsMinimum
15 H-1B approvalsDept. of Labor
3 green cardsCertified filings
GxP Compliance and RegulationsElectronic Lab Notebooks (ELN)Revvity SignalsSoftware Development Life Cycle (SDLC)Agile MethodologyWaterfall MethodologyJiraConfluenceScientific Workflow ImplementationData GovernanceFAIR Data PrinciplesLife Sciences

About the company

InterSources Inc logo
InterSources Incintersourcesinc.com

InterSources Inc. solves operational problems where protection, performance, compliance, AI, and workforce capability must work together.

Visa sponsorship history

4 years sponsoring, last filed FY2026

Data powered by U.S. Department of Labor. This does not guarantee sponsorship for this specific role.
15H-1B approved
100%approval rate
3new H-1B hires
3PERM certified
$103,979median wage / yr
H-1B Petition ApprovalsVisas USCIS actually granted: the strongest sign the company sponsors.
20232
20247
20255
20261
LCA Certified ApplicationsAn early filing step, not a visa approval: it signals intent, not confirmed sponsorship.
20239
20244
20251
20261
Green Card (PERM) FilingsCertified green card filings: a long-term commitment to international hires.
20231
20241
20251
Top sponsored roles
SOFTWARE QUALITY ASSURANCE ENGINEERSOFTWARE DEVELOPERBUSINESS ANALYSTTECHNICAL RECRUITERSYSTEMS ENGINEER
Sponsored employees from
India

Job description

Summary

The company is seeking an ELN Signals Product Analyst to support the implementation and optimization of electronic laboratory notebook workflows in GxP-regulated life sciences environments. The role translates scientific processes into technical requirements, manages SDLC activities, ensures compliance and data integrity, and supports validation, testing, governance, and downstream analytics integration.

Responsibilities

  • Translate scientific research processes into actionable technical requirements for electronic laboratory notebook systems (e.g., Revvity Signals)
  • Execute end-to-end SDLC activities, supporting both Agile and Waterfall release management using Jira, Confluence, and designated testing tools
  • Ensure strict compliance with GxP regulations and internal IT quality standards throughout all system lifecycle phases
  • Collaborate with business stakeholders, lab end-users, and technical engineering teams to refine business drivers and operational deliverables
  • Partner with downstream reporting and analytics teams to support scientific data governance and structured data integration
  • Drive validation testing, requirement traceability, and user testing scripts for platform updates
  • Lead requirements gathering and business process mapping for laboratory digital tools
  • Drive GxP compliance and system validation throughout software delivery lifecycles
  • Author user stories, operational test cases, and technical documentation using Jira and Confluence
  • Partner with reporting and analytics teams to support lab data governance and downstream integrations

Skills

  • GxP Regulations (3+ years) – Practical application in IT systems, regulatory compliance, and validation documentation within life sciences
  • Electronic Lab Notebooks / ELN (3+ years) – Direct, hands-on experience using and configuring e-notebook software (specifically Revvity Signals)
  • SDLC Execution (3+ years) – Proficient in requirements gathering, user testing, and managing work item traceability in Jira and Confluence under Agile and Waterfall paradigms
  • Inability to work EST core business hours or lack of proximity to Rahway, NJ / East Coast facilities
  • Lack of hands-on experience with Electronic Lab Notebooks (ELN) or GxP-regulated IT environments
  • Inability to demonstrate structured SDLC documentation and testing experience using Jira/Confluence
  • GxP Compliance & Regulations (3+ years)
  • SDLC Methodologies (Agile & Waterfall) utilizing Jira & Confluence (3+ years)
  • Work setup: Remote, (preference to be co-located near Merck East Coast facilities or working strict EST hours)
  • Hands-on experience with Electronic Lab Notebooks (Revvity Signals preferred) (3+ years)
  • End-to-end scientific workflow implementation in e-notebooks or lab systems
  • Knowledge of data governance and FAIR data principles
  • Downstream dashboard, analytics, and reporting integration experience
  • Biotechnology / Life Sciences domain experience

Qualifications

Must Haves

  • GxP Regulations (3+ years) – Practical application in IT systems, regulatory compliance, and validation documentation within life sciences
  • Electronic Lab Notebooks / ELN (3+ years) – Direct, hands-on experience using and configuring e-notebook software (specifically Revvity Signals)
  • SDLC Execution (3+ years) – Proficient in requirements gathering, user testing, and managing work item traceability in Jira and Confluence under Agile and Waterfall paradigms
  • Inability to work EST core business hours or lack of proximity to Rahway, NJ / East Coast facilities
  • Lack of hands-on experience with Electronic Lab Notebooks (ELN) or GxP-regulated IT environments
  • Inability to demonstrate structured SDLC documentation and testing experience using Jira/Confluence
  • GxP Compliance & Regulations (3+ years)
  • SDLC Methodologies (Agile & Waterfall) utilizing Jira & Confluence (3+ years)

Nice to Haves

  • Work setup: Remote, (preference to be co-located near Merck East Coast facilities or working strict EST hours)
  • Hands-on experience with Electronic Lab Notebooks (Revvity Signals preferred) (3+ years)
  • End-to-end scientific workflow implementation in e-notebooks or lab systems
  • Knowledge of data governance and FAIR data principles
  • Downstream dashboard, analytics, and reporting integration experience
  • Biotechnology / Life Sciences domain experience

Benefits

  • Remote work setup, with preference for candidates co-located near Merck East Coast facilities or working strict EST hours

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