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Technical Analyst Assay Registration Aws Spotfire

Posted on: Nov 12, 2026

Gandiva Insights
Jersey City, New Jersey
Remote
CTC

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Job Title :

Technical Analyst Assay Registration Aws Spotfire

Job Type :

Contract

Job Location :

Jersey City New Jersey United States

Remote :

Yes

Job Description :

Title: Technical Analyst Assay Registration, AWS & Spotfire

Location: Remote / New Jersey (NJ)
Duration: 12 Months Contract

Note : W2 only [No C2C]

Skills: Configure in vitro assays, model scientific, clinical and safety data, and develop Spotfire dashboards for R&D, pharmacovigilance and operations. Deliver compliant data solutions using Agile practices.

Job Summary:

We are looking for an experienced Technical Analyst Assay Registration, AWS & Spotfire to support scientific data management, assay registration, and analytics initiatives. The ideal candidate should have experience configuring in vitro assays, modeling scientific, clinical, and safety data, and developing interactive dashboards using TIBCO Spotfire.

The candidate will work closely with R&D, Pharmacovigilance, and Operations teams to deliver scalable, compliant, and data-driven solutions using Agile methodologies.

Key Responsibilities:

Configure, manage, and maintain in vitro assay registration and associated scientific data.
Model and manage scientific, clinical, and safety-related data to support R&D initiatives.
Develop interactive dashboards, visualizations, and analytical reports using TIBCO Spotfire.
Leverage AWS cloud services to support scientific data solutions, data integration, and analytics.
Collaborate with R&D, Pharmacovigilance, and Operations teams to understand business and technical requirements.
Support data integration, transformation, validation, and reporting activities.
Ensure data quality, accuracy, consistency, and compliance with applicable regulatory standards.
Translate business requirements into technical specifications and analytical solutions.
Participate in Agile ceremonies, including sprint planning, daily stand-ups, and sprint reviews.
Troubleshoot technical issues and continuously improve data workflows and reporting solutions.

Required Skills & Qualifications:

Experience in Assay Registration and In Vitro Assays.
Strong understanding of scientific, clinical, and safety data modeling.
Hands-on experience with TIBCO Spotfire dashboard development and data visualization.
Experience with AWS cloud services and cloud-based data solutions.
Knowledge of data integration, data transformation, and data management processes.
Understanding of R&D, Pharmacovigilance, and pharmaceutical/biotechnology workflows.
Experience delivering compliant data solutions in regulated environments.
Familiarity with Agile/Scrum methodologies.
Strong analytical, communication, and problem-solving skills.

Preferred Qualifications:

Experience in pharmaceutical, biotechnology, or life sciences domains.
Exposure to scientific data platforms and laboratory data management.
Understanding of GxP and regulatory compliance requirements.

Position Details

Posted:

Nov 12, 2026

Reference Number:

616-36218

Employment:

CTC

City:

Jersey City

Job Origin:

CIEPAL_ORGANIC_FEED

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