Master Data Specialist, Engineering (Onsite)

Job Description Applications are sought for an SAP Master Data Specialist in Vaccines and Advanced Biotechnologies Process R&D (VAX PR&D). This role supports pilot‑scale GMP manufacture of bulk biologic clinical supplies (vaccines and therapeutic proteins) and will create, design, and sustain standardized business processes, master data management, system sustainment, and lifecycle material management, while providing support for peer coaching and consultation as needed. The position will be temporarily based in West Point, PA for approximately 18 months (up to 24 months). After this period, the role is intended to relocate to Rahway, NJ. Applicants should be comfortable with this planned geographic transition. The role will be part of the VAX PR&D Planning and Manufacturing Systems (PAMS) team before transitioning to support the Next Generation Biologics (NGB) facility— a forthcoming state‑of‑the‑art, multi‑product GMP site at the CMC hub in Rahway, NJ. Location and Duration Temporary location: West Point, PA for 18 – 24 months, followed by relocation to Rahway, NJ. Responsibilities Support the creation, maintenance, review, analysis, and accuracy of master data. Assist in the sustainment, performance, and monitoring of standard business processes in all production execution and master data functions. Support master data governance activities, including adherence to data standards, stewardship expectations, and escalation processes. Gather, analyze, and report process performance and transactional discipline metrics to support compliance and continuous improvement efforts. Collaborate with site and regional/global team members and participate as a member of the site CoP Team as needed. Assist in the development and maintenance of SOPs and training materials and provide end‑user training support. Identify, troubleshoot, and help resolve master data issues, escalating more complex issues as needed. Participate in process improvement projects and support project planning, stakeholder coordination, and implementation activities. Identify and support continuous process improvement opportunities and help promote best practices across the network. Coordinate and share best practices with our company sites in the network. Serve as a technical resource to team members by providing consultation, coaching, and practical support within area of expertise. 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 2 full years of relevant experience or a Master’s degree with 1+ year 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. 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. Salary The salary range for this role is $87,300.00 – $137,400.00. Benefits We offer a comprehensive package of benefits, including medical, dental, vision, and other insurance, as well as retirement benefits (401(k)), paid holidays, vacation, and compassionate/sick days. For more information, visit Equal Employment Opportunity and Accommodations 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. 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