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Senior Specialist, Technical Product Analyst

Job in Rahway, Union County, New Jersey, 07065, USA
Listing for: MSD Malaysia
Full Time position
Listed on 2026-08-30
Job specializations:
  • IT/Tech
    IT Business Analyst, Business Systems & Technology Analysis
  • Business
    Business Systems & Technology Analysis
Salary/Wage Range or Industry Benchmark: 117000 - 184200 USD Yearly USD 117000.00 184200.00 YEAR
Job Description & How to Apply Below

Job Description

Functional Area:

Digital Regulatory & Safety within Clinical Development and Digital Solutions (CDDS) The Regulatory Document Lifecycle Management Product Team serves as a strategic business partner, collaborating across IT, business, and vendor teams to deliver innovative digital capabilities that support Regulatory Operations and improve business productivity. We are seeking a detail-oriented and highly motivated Technical Product Analyst with a strong blend of product analysis, business analysis, technical aptitude, and domain knowledge.

This role will support the ongoing delivery, optimization, and growth of regulatory lifecycle and document management capabilities, with a focus on business process analysis, requirements management, solution configuration awareness, SDLC adherence, and delivery of high-quality outcomes in a regulated environment.

Senior Specialist, IT – RDLM Product Team

Job Summary The RDLM Product Team serves as a strategic business partner, collaborating across IT, business, and vendor teams to deliver innovative digital capabilities that support Regulatory Operations and improve business productivity. We are seeking a detail-oriented and highly motivated Senior Specialist, IT with a strong blend of product analysis, business analysis, technical aptitude, and domain knowledge. This role will support the ongoing delivery, optimization, and growth of regulatory lifecycle and document management capabilities, with a focus on business process analysis, requirements management, solution configuration awareness, SDLC adherence, and delivery of high-quality outcomes in a regulated environment.

Primary

Responsibilities
  • Partner with business stakeholders, product owners, IT teams, and vendors to understand business needs, product priorities, and end-to-end regulatory lifecycle and document management processes.
  • Gather, analyze, and document business requirements, process flows, user stories, acceptance criteria, and functional specifications to support product capabilities and enhancements.
  • Serve as a liaison between business and technical teams, translating business needs into clear, actionable solution requirements.
  • Support product roadmap execution by collaborating with product management and delivery teams to align scope, priorities, releases, and technical capabilities.
  • Analyze current-state processes and identify opportunities for simplification, standardization, automation, and continuous improvement.
  • Develop a comprehensive understanding of business processes and data flows, including inputs and outputs, related to Veeva RIM Submissions and Archive capabilities.
  • Utilize JIRA to manage requirements, track work items, support traceability, and document delivery progress throughout the project lifecycle.
  • Stay informed about industry trends, best practices, and emerging capabilities in regulatory and life sciences technology, and apply this knowledge to help drive product innovation and continuous improvement.
Qualifications
  • Bachelor’s degree in information technology, Business Administration, Computer Science, or related discipline.
  • Minimum of 5 years of relevant experience in product analysis or business analysis, preferably within the life sciences or healthcare industry.
  • Proven track record of managing complex projects and working collaboratively in cross-functional teams.
  • Strong understanding of the software development lifecycle (SDLC) and delivery methodologies, including Agile, Waterfall, and Kanban.
  • Excellent communication and interpersonal skills, with the ability to tailor messages to different audiences and build strong working relationships.
Preferred Qualifications
  • Hands‑on experience with Veeva RIM or another regulatory information management system is highly desirable.
  • Familiarity with regulatory lifecycle management, health authority interactions, or related regulatory operations processes.
  • Experience with JIRA for backlog management, requirements tracking, and delivery documentation.
  • Familiarity with GxP, GMP, and best practices for implementing and maintaining highly compliant systems.
  • Project management, Agile, Product Owner, Business Analysis, or…
Position Requirements
10+ Years work experience
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