Signals Technical Analyst/ELN Analyst

Title: Signals Technical Analyst/ELN Analyst
Location: Rahway, NJ Onsite
Duration: 6+ Months of Contract

Must-Have Skills:
Signals Technical Analyst / ELN Analyst to support Revvity (PerkinElmer) Signals, which is an Electronic Laboratory Notebook (ELN) used in pharma R&D and manufacturing.
They want someone who can bridge business, scientific users, and IT, while ensuring everything is GxP-compliant.
It is a functional / technical analyst + product role.



The person will:
Work closely with Product Managers and Product Owners
Translate scientific & business needs into system requirements
Support, configure, and enhance the Revvity Signals ELN platform
Ensure regulatory compliance (GxP) throughout the system lifecycle



Job Description:
The IT Product Analyst will collaborate with the Product Owner and Product Management team, reporting to the Product Manager of Assay Data Processing. This role serves as a key liaison between business stakeholders and technical teams to support and enhance digital solutions within the pharmaceutical R&D and manufacturing domains.
The focus is on GxP-compliant systems and electronic laboratory notebooks (e-notebooks), ensuring that solutions meet both regulatory standards and the scientific needs of diverse users.



Key Responsibilities:
Collaborate with cross-functional teams to gather, analyze, and document business requirements for GxP-regulated systems .
Hands-on experience with electronic laboratory notebooks ( Revvity Signals).
Support the implementation, configuration, and lifecycle management of e-notebook solutions (e.g., Revvity Signals or similar).
Ensure systems and processes comply with GxP regulations, including validation, audit readiness, and data integrity.
Act as a product owner or SME for assigned digital solutions, driving enhancements and resolving issues.
Partner with Quality Assurance and Regulatory teams to support compliance activities, including change control and User Acceptance Test processes.
Facilitate user acceptance testing (UAT), training, and onboarding for new features and system upgrades.
Monitor user feedback to identify opportunities for continuous improvement.
Maintain full SDLC documentation set, for example user stories, functional specifications, SOPs, and validation liverables.



Qualifications:
Bachelor's degree or equivalent professional experience in Computer Science, Life Sciences, Information Systems, or related field.
3+ years of experience in IT business analysis or product management within the pharmaceutical or life sciences industry.
Strong understanding of GxP regulations and their application in IT systems.
Familiarity with SDLC methodologies, including Agile and Waterfall. This would include hands on experience with Jira, testing tools, and Confluence applications.
Excellent communication, stakeholder management, and problem-solving skills.
Experience with validation documentation and audit support is a plus.