Associate Director, Technical Product Management

Job DescriptionOur IT team operates as a business partner proposing ideas and innovative solutions that enable new organizational capabilities. We collaborate internationally to deliver the services and solutions that help everyone to be more productive and enable innovation.The Information Technology team at our Research & Development Division is looking for Product Manager – PV Reporting and Surveillance. Reporting into the Product Line Lead for Clinical Safety. The position will take a leadership role in the development and implementation of pharmacovigilance strategies, processes, and systems for a pharmaceutical company, ensuring compliance with regulatory requirements and maintaining high-quality standards.Product managers must possess a broad base of skills and knowledge spanning digital technology, strategy and business planning, user experience design, engineering, and agile/lean development practices. They must possess an entrepreneurial drive to develop new product features while managing stakeholders’ needs and timeframes to broker complex relationships that evolve into real solutions. The ultimate success of a product owner hinges on their ability to guide their peers while influencing decisionmakers.What will you do?Partner with cross-functional teams to develop and implement pharmacovigilance (PV) strategies that meet regulatory requirements and ensure patient safety, quality, and compliance.Manage and prioritize the product backlog, ensuring business value is understood and aligned with organizational objectives.Develop, maintain, and execute the Product Strategy and Roadmap.Oversee pharmacovigilance systems, including software platforms used for adverse event reporting, case management, and signal detection.Maintain current knowledge of global pharmacovigilance regulations and guidelines and ensure company PV processes and systems remain compliant.Ensure pharmacovigilance processes and systems adhere to applicable regulatory requirements, including International Council for Harmonisation (ICH) guidelines.Maintain high-quality standards for PV processes and systems and implement quality control measures to ensure data accuracy, integrity, and compliance.Collaborate with Clinical, Regulatory, Safety, and other key functional areas to integrate pharmacovigilance processes into overall product development plans.Partner with Business Technology teams to manage the implementation of new PV/QC systems and enhancements, ensuring project milestones and timelines are achieved.Build and maintain strong stakeholder relationships to support effective decision-making, alignment, and execution across functions.Demonstrate strong stakeholder management skills, including communication, influence, and cross-functional collaboration.Qualifications, Skills & Experience RequiredBachelor’s degreeSix or more (6) years of experience in data governance, compliance, privacy, risk management, AI governance, or related rolesStrong communication skills with both technical and non-technical audiencesExperience with data governance, data products, digital solutions, and Agentic AI-enabled programsAbility to develop policies, standards, SOPs, and governance processesWorking knowledge of data management practices, including data quality, metadata, security/privacy, and master data managementAbility to identify and manage governance, compliance, privacy, and risk issuesStrong collaboration and influencing skills across cross-functional teamsAbility to drive change, continuous improvement, and adoption of governance practicesStrong writing, organization, and problem-solving skillsAbility to work effectively in a fast-paced, ambiguous, and evolving environmentUnderstanding of healthcare compliance laws, regulations, and guidelinesExperience developing and delivering training and guidance to a broad audienceAbility to build trusted relationships with internal and external stakeholdersPreferredMaster’s degree, MBA, or equivalentExperience supporting IT, data, analytics, or AI solutions in a complex or regulated environmentExperience with privacy and data protection practicesExperience supporting compliance training, reporting, and remediation activitiesExperience in healthcare or life sciencesExperience with quality management systemsPharmacovigilance compliance experienceWhat we offerExciting opportunities to work as part of a high-performing team on global projects within an international environment.Opportunities for continuous learning and professional growth, with the potential to develop a career across the company’s global organization.SWE2026Required Skills: Data Quality Assurance, Management System Development, Pharmaceutical Regulatory Compliance, Pharmacovigilance, Photovoltaic Systems, Product Development, Product Management, Quality Control (QC), Safety Cases, Signal Detection Theory (SDT), Solution Architecture, Stakeholder Relationship Management, Strategic Planning, System Designs, VeevaPreferred Skills: Current Employees apply HERECurrent Contingent Workers apply HEREUS 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.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 RightsEEOC 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 ActsThe primary location for this posting is:USA - New Jersey - RahwayWhere required by law, the compensation range for this role is provided below.The salary range for the primary location of this role is:$142,400.00 - $224,100.00This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of 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 .Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location.Additional location(s) Compensation Information:San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance OrdinanceLos 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 OrdinanceSearch Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: RegularRelocation:No relocationVISA Sponsorship:NoTravel Requirements:10%Flexible Work Arrangements:HybridShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aJob Posting End Date:11/6/2026*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. SummaryLocation: USA - New Jersey - Rahway; USA - Pennsylvania - North Wales (Upper Gwynedd)Type: Full time