Senior Specialist, Technical Product Analyst

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. 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 life cycle (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 Veeva-related certification is a plus. Strong analytical mindset with effective problem‑solving skills. Required Skills Change Catalyst, Cloud Computing, Customer‑Focused, Demand Management, End User Computing, Group Policy Management, ITIL Service Delivery, IT Infrastructure Management, Network Administration, Object‑Oriented Programming (OOP) Concepts, Professional Etiquette, Server Hardware Configuration, Software Development, Sourcing Services, Strategic Planning US And Puerto Rico Residents Only Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. Requirements As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $117,000.00 - $184,200.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Employee Status Regular Flexible Work Arrangements Hybrid Job Posting End Date 09/10/2026 A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID: R414255 #J-18808-Ljbffr Merck