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At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
R&D Operations
Job Sub Function:
Clinical Supply Operations:
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium, Horsham, Pennsylvania, United States of America, Malvern, Pennsylvania, United States of America
Job Description: About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
US - Requisition Number: R-070534
- Belgium
- Requisition Number: R-069385
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
We are searching for the best talent for a Senior Analyst, Transcend R&D CMMSrole in Beerse, Belgium or U.S. (Malvern, PA or Horsham, PA).Purpose:
Innovative Medicine Transcend is a global business transformation program that will modernize our foundational Supply chain processes and harmonize them into one “clean” ERP as a standardized platform (SAP S4 Hana) for growth and efficiency gains.
The program will simplify the Pharm ERP landscape from 7 to 1, standardizing processes to have a cost effective, fit for purpose digital backbone that will enable us to support the Pharm business with agility.
R&D is an integral part of the IM Transcend program, in order to transform and standardize relevant R&D supply chain processes, to include them within the global IM Transcend Template.
The Transcend R&D program team is now looking for a Senior Analyst,Transcend R&D CMMS, responsible for leading the CMMS deliverables within R&D as part of the Transcend (SAP S/4HANA) transformation. This role ensures the end-to-end design, data readiness, integration alignment, and deployment execution for computerized maintenance management processes and related assets, enabling compliant, reliable maintenance operations and inspection readiness across R&D sites.
The position will be reporting into the Transcend R&D manufacturing implementation lead.
You will be responsible for:
-
Lead CMMS process and solution alignment within the global template and deployment model (asset hierarchy, work management, preventive maintenance, calibration/inspection where applicable).
-
Own CMMS requirements and backlog for R&D, ensuring traceability through design, build, test, and release; drive decisions and manage escalations.
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Coordinate CMMS master data and migration readiness (equipment/asset data, task lists, plans, BOMs/spares where applicable), including reconciliation and sign-off.
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Partner with integration and architecture teams to ensure end-to-end flows between SAP S/4HANA, other platforms, and site systems.
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Drive test strategy and execution readiness (BST/UAT), including defect triage, business validation, and operational readiness.
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Embed compliance-by-design: partner with Technology Quality/CSV and Quality/Compliance to ensure controlled processes, documentation, and audit-ready evidence.
-
Support cutover planning and hypercare stabilization for CMMS capabilities; ensure smooth transition to support/operations.
-
Lead change management inputs (training needs, SOP impacts, role mapping) in collaboration with business adoption teams.
Approximate Percentage of Time & Tasks/Duties/Responsibilities:
-
25% Process/solution leadership and governance (requirements, decisions, dependency management).
-
20% Data readiness and migration coordination (asset/equipment data, plans, reconciliation, sign-offs).
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20% Testing and validation readiness (BST/UAT support, defect triage, business validation).
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15% Integration alignment and end-to-end scenario assurance.
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10% Cutover and hypercare execution/stabilization.
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10% Compliance and documentation management (CSV/SDLC evidence, SOP impacts, audit readiness).
Other responsibilities:
-
Support audits/inspections and contribute to CAPA planning and execution related to maintenance system processes.
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Contribute to continuous improvement of CMMS templates, playbooks, and operational controls for future deployments.
Required Qualifications:
-
Bachelor’s degree or equivalent experience: Business Engineering, Life Sciences, Information Systems, or related discipline.
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5+ years of experience in maintenance management/CMMS, asset management processes, and/or plant/site/lab operations.
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Experience with ERP-enabled maintenance processes (SAP PM) and end-to-end work management lifecycle.
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Proven experience working in a GxP regulated environment
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Strong understanding of controlled documentation practices and compliance expectations for computerized systems in regulated environments.
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Demonstrated ability to lead cross-functional delivery across process, data, and technology teams, including asset structures and preventive maintenance
-
Strong communication and stakeholder management skills; ability to drive decisions and manage competing priorities
Preferred Qualifications:
-
Experience delivering transformations using Agile/PI planning and global template deployments.
-
Cross-functional exposure
-
Agile methodology
-
Use of Jira
-
Travel up to 10%
Key Working Relationships:
-
MAKE pillar leadership Transcend; R&D site maintenance/engineering leaders and SMEs.
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Global template teams (process owners, template owners/managers) and deployment leads.
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IT delivery teams (solution architecture, integration, data migration, testing, cutover, support).
-
Quality/Compliance partners (Technology Quality/CSV, GxP as applicable) and ISRM.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.
Required Skills: Preferred Skills:
Analytical Reasoning, Clinical Supply Chain, Clinical Trials Operations, Communication, Distribution Management, Inventory Control, Inventory Optimization, Laboratory Operations, Mentorship, Organizing, Package and Labeling Regulations, Problem Solving, Process Improvements, Project Management, Research and Development, Stakeholder Engagement, Standard Operating Procedure (SOP)
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Johnson & Johnsonについて

Johnson & Johnson
PublicCaring for the world, one person at a time.
10000+
従業員数
New Brunswick
本社所在地
$400B
企業価値
レビュー
4.0
10件のレビュー
ワークライフバランス
3.5
報酬
4.2
企業文化
4.1
キャリア
3.2
経営陣
4.3
75%
友人に勧める
良い点
Supportive and approachable management
Excellent benefits and compensation
Flexible work arrangements and good work-life balance
改善点
High-pressure and demanding work environment
Slow bureaucratic processes
Limited growth opportunities in some areas
給与レンジ
2,250件のデータ
Mid/L4
Senior/L5
Director
Mid/L4 · Manager
338件のレポート
$155,591
年収総額
基本給
$137,488
ストック
-
ボーナス
$18,103
$106,549
$229,934
面接体験
7件の面接
難易度
3.0
/ 5
期間
14-28週間
面接プロセス
1
Application Review
2
HR Screen
3
Pre-recorded/Video Interview
4
Technical/Panel Interview
5
Final Interview
6
Offer
よくある質問
Behavioral/STAR
Technical Knowledge
Past Experience
Culture Fit
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