Master Data Specialist, Engineering (Onsite)

Job Description Specialist — BPP to NGB Pilot Plant Master Data (SAP) Our Research Scientists are our Inventors. We identify and target steps in disease mechanisms or pathways that could be inhibited or enhanced. Our goal is to isolate a compound that is effective against a disease target. Using innovative thinking, state-of-the-art facilities and robust scientific methodology, we collaborate to discover the next medical breakthrough. Applications are sought for an SAP Master Data Specialist in Vaccines and Advanced Biotechnologies Process R&D (VAX PR&D). The 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) 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. This 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. NGB will enable flexible multi-suite operations across development and pilot scales, support potent-material handling, and integrate novel cell-line and technology platforms. The Biologics Process R&D organization develops drug-substance manufacturing processes across biotherapeutic modalities and partners with Discovery, Pre‑clinical, Early Development, and Manufacturing to enable clinical supply and commercial launches, including implementation of new technologies and scalable processes. The SAP Master Data Specialist will use SAP, business process knowledge, and SOPs to maintain alignment with global business processes and site regulatory requirements. The successful candidate will work closely with Process Staff, Formulators, Engineers, IT, Quality, and other team members to understand and execute master data requirements, support cross‑functional initiatives, and contribute to continuous improvement. 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 Master’s degree with 1+ year of relevant experience 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 Required Skills cGMP 지침 cGMP 지침

GMP 준수

SAP PP(생산 계획)

개인 이니셔티브

구두 커뮤니케이션

규제 요구사항

기술 플랫폼

데이터 거버넌스

멸균 제조

문제 해결

비즈니스 프로세스

생산 계획

시험 공장 운영

실험실 실험

우선순위 적응성

전자 배치 기록

제품 구축

지속적인 프로세스 개선

치료용 단백질

테크니컬 라이팅

팀워크

포유류 세포 배양

표준 운영 절차(SOP) 작성 {+ 2 more} The salary range for this role is $87,300.00 - $137,400.00. 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. Benefits medical, dental, vision healthcare and other insurance benefits (for employee and family) retirement benefits, including 401(k) paid holidays vacation compassionate and sick days 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. 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. 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 Search 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. 당사는 글로벌 헬스케어 리더로서 다양한 처방약, 백신 및 동물 건강 제품 포트폴리오를 가지고 있습니다. 잠재력과 성공 사이의 차이는 혁신과 창의력을 일깨우는 불꽃에 있습니다. 이는 백년이 넘는 세월 동안 우리가 유산으로 지켜온 신조입니다. 우리의 성공은 윤리적 성실성, 전향적인 모멘텀, 그리고 글로벌 헬스케어에서 새로운 이정표를 세우겠다는 고무적인 임무에 의해 가능해 집니다. #J-18808-Ljbffr MSD Malaysia