Sr. Spclst, Engineering

Job Description Applications are sought for an SAP Master Data Sr. Specialist in Vaccines and Advanced Biotechnologies Process R&D (VAX PR&D). The role supports pilot‑scale GMP manufacture of bulk biologic clinical supplies and will create, design, and sustain standardized business processes, master data governance, system sustainment, and lifecycle material management, while providing peer coaching and expert consultation. The position will be temporarily based in West Point, PA for approximately 18 months (up to 24 months) to support business needs. After this period, the role is intended to relocate to Rahway, NJ. Applicants should be comfortable with this planned geographic transition. Responsibilities Act as the Master Data subject matter expert and apply advanced knowledge to the creation, maintenance, review, analysis, and accuracy of master data. Design, implement, sustain, and monitor standard business processes in all production execution and master data functions. Own and drive master data governance activities, including definition of data standards, stewardship roles, and escalation paths. Gather, analyze, and report process performance and transactional discipline metrics to ensure compliance and continuous improvement; translate metrics into action plans. Collaborate with other site and regional/global team members and participate as a member of the site CoP Team; influence regional master data strategies. Develop and maintain SOPs along with associated trainings and provide delivery of the end‑user trainings; lead change management activities. Identify, troubleshoot, and resolve complex master data issues and lead root‑cause corrective actions. Lead and assist in process improvement projects; manage project planning, stakeholder engagement, and delivery of outcomes. Identify and implement continuous process improvement opportunities and promote best practices across the network. Coordinate and share best practices with our company sites in the network. Act as a resource for technical expertise—offering consultation, coaching, and practical support to team members at all levels. Assist in external agency inspections, as needed. Support safety, compliance, and GMP initiatives. Qualifications BS degree in Engineering, Sciences, Business, or a related field with minimum 5 years of relevant experience or a Master’s degree with 3 years of relevant experience. Required Experience And Skills Ability and desire to work in a fast‑paced and dynamic pilot plant environment that demands out‑of‑box thinking, prioritization, and rapid response to events and situations. Direct experience with working with SAP master data. Strong understanding of manufacturing principles/processes through work experience and ability to translate manufacturing requirements into an automation/digital solution. Experience leading projects and influencing stakeholders across functions in a challenging and changing global environment. Ability to work collaboratively as part of a team across various functions in a challenging and changing global environment. Proven track record of analytical skills, problem solving, and attention to detail. High personal integrity, credibility, and energy. Strong written and verbal communication skills. Strong computer skills in Excel. Preferred Experience And Skills Experience in pharma/sterile manufacturing. Experience in working with MES systems. Prior experience mentoring or supervising other specialists, and driving cross‑site initiatives. Equal Employment Opportunity 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 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 The salary range for this role is $117,000.00 - $184,200.00. The successful candidate will be eligible for an annual bonus and long‑term incentive, if applicable. 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. Requisition ID: R395896 Job Posting End Date: 06/5/2026 #J-18808-Ljbffr Merck