Signals Technical Analyst​/ELN Analyst

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 (Perkin Elmer) 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