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About the Job

Sanofi Manufacturing and Supply organization is preparing its future through an ambitious program named Modulus. The Modulus Project is at the cornerstone of Sanofi strategy as it aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable and agile, leveraging new disruptive technologies, to better address vaccine business challenges as well as Specialty Care Biologics products.

Main Accountabilities

• Administer, maintain, and troubleshoot the Kepware connectivity platform and the Aspen IP.21 real-time database.

• Configure new devices, tags, and data flows within Kepware to integrate data from PLCs, DCS and analytical equipment.

• Design, develop, and maintain robust data extraction and transformation logic using Aspen SQLplus to create reliable data feeds for Manufacturing Execution Systems (MES) and other business applications.

• Ensure reliable and secure data flow from OT-level systems (via Kepware) to the IP.21 historian and other IT-level systems.

• Implement system change controls, upgrades, perform backups, and ensure system security and compliance with GMP requirements and industry standards.

• Create and maintain documentation for system configurations, interfaces, and standard operating procedures.

• Collaborate with cross-functional teams to support process optimization, troubleshooting, and regulatory compliance initiatives.

• Provide SME support for deviation root cause analysis.

Key roles (D,.A,.I)

• D: Decide on specific configuration parameters for tags, devices, and channels within Kepware and data points within IP.21, adhering to established architecture.

• D: Determine the technical approach, writing, and optimization of SQLplus queries and scripts for data extraction and transformation.

• D: Make immediate decisions during incident response and execute standard operational procedures for system health and recovery.

• A: Advise on system architecture, technology upgrades, capacity planning, and the introduction of new drivers or integration tools.

• A: Provide technical analysis and recommendations for new projects and major changes, including risk assessments and implementation plans.

• A: Develop and propose SOPs, backup strategies, and contribute to GxP validation documentation.

• I: Be informed of team goals, priority shifts, and relevant decisions from other IT/OT projects that may impact the data systems.

• I: Receive regular performance feedback and be notified of major team-wide incidents or approved changes.

Expected Experience

• Minimum 8 years' experience in administering, configuring, and troubleshooting the Kepware (KEPServerEX) platform and AspenTech IP.21 real-time database.

• Practical background in supporting OT/IT data infrastructure within a GxP-regulated environment, with a clear understanding of data integrity and GMP standards.

• Experience in DeltaV DCS or Siemens PLC/WinCC.

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About the job

We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Sanofi has added two new Modulus Facilities to our global industrial footprint. These production units represent the future of manufacturing. They allow us to increase our capacities while making production more flexible and respectful of the environment.

Fully digitalized, our Modulus Facility will enable more responsive and flexible manufacturing across multiple vaccine and biological platforms including mRNA, while minimize our impact to the environment. Our Modulus Facilities will help improve people’s lives by giving them faster access to more treatments

In this context, we are looking for one Quality Control Specialist to participate in the setting up of the new QC laboratory for our new site based in Singapore.

Key Accountabilities

The mission described below, must be exercised in compliance with health, safety and environment of the site rules.

• Support the set up and routine operations of the new QC laboratory based in Singapore:

• Support the project execution phase through deliverables achievement and operations activities

• Write and review key documents relating to QC (such as URS, plans, protocols, reports, SOPs, risk assessments)

• Review and approve vendor supplied documents

• Support the laboratory start-up activities, participate and/ or provide oversight to the C&Q and validation activities

• Participate in method verification for bioburden and endotoxin tests or environmental monitoring related study.

• Perform aseptic sample dispensing

• Perform QC microbiological test for water, raw materials and product samples

• Perform growth promotion test and microbial identification

• Perform environmental monitoring and clean utilities sampling including WFI, clean steam and clean gases

• Train newcomers for QC lab activities and testing

• Participate and contribute to laboratory continuous improvement

• Contribute to laboratory performance (eg, deviation/OOS rate, sample turnaround time)

• Ensure the consistency of practices between EVF project ambition, QC Center of Excellence roadmap including new technology and Sanofi Guidelines and ensure the connection with the QC Sanofi network.

• Contribute to reach the EVF quality manufacturing 4.0 ambition through a Quality plan.

• Support the Team in case of Health Authorities communication.

• Ensure Continuous Quality Improvement in the QC laboratories.

About You

Education and experience

• Bachelor’s or Master’s Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology with about 3-7 years of experience in QC lab operations and testing.

• Experience in microbiological method verification and microbial identification in the pharmaceutical or biotechnology industry preferred.

Key technical competencies and soft skills:

• Manufacturing 4.0 mindset (such as Agile methodology)

• Knowledge of regulations and standards of the pharmaceutical industry, Global Quality policies and Data Integrity Requirements.

• Knowledge of the quality systems and associated technologies.

• Good understanding of good laboratory practices, good documentation practice and data integrity requirements.

• Strong interpersonal relationships to establish the partnerships necessary for the development of the Quality culture.

• Discipline and assertiveness in the decision-making and execution in laboratory start-up activities.

• Good communication skills to advocate QC positions with other functions, including during inspections.

• Experienced in routine laboratory operations and continuous improvements.

• Experienced in start-ups will be advantageous.

• Keen to learn new technologies.

• Fluent in English speaking and writing.
  
   

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Job title: Senior Technician I, Maintenance

• Location: Singapore

• Hiring Manager: Process Engineer

About the Job:

We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.

Main responsibilities:

Vaccines M&S is preparing its future through an ambitious program named Evolutive Facility (EVF). The EVF Project is at the cornerstone of Sanofi strategy as it aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable, and agile, leveraging new disruptive technologies, to better address vaccine business challenges.   

An EVF Senior Maintenance Technician is responsible for ensuring the smooth and efficient operation of equipment, maintenance tasks, and facilities. They also assist with equipment maintenance setup and support during the greenfield project phase and operational start-up.

The technician will be guided by the EVF Engineering Maintenance Engineer for all job-related activities and will report to the Maintenance EFU Manager

1. Operation and Maintenance of black / clean utility systems and single use equipment (20%)

• Perform routine preventive and ad-hoc maintenance on clean and black utilities, and single-use manufacturing equipment, such as bioreactors, UFDF systems, biosafety cabinets, centrifuges, column packing units, autoclaves, washers, dispensing booths, and similar equipment.

• Proficient in the operation and maintenance of Clean and Black utility systems and infrastructure services, including chilled water systems, compressed air systems, water systems, steam systems, waste management, RO water, water for injection, clean gases, and solvent systems.

• Ensure all operation and maintenance activities are meticulously documented to demonstrate compliance with regulatory requirements.

• Assist production teams by troubleshooting problems, resolving issues, and assessing situations to determine when escalation to higher-level support is necessary.

•  Possess knowledge of valve maintenance and repair, including PSV, GEMU, control valves, pinch valves, butterfly valves, check valves, and others.

2. People Management (10%)

• Oversee and manage contractors or vendors, to ensure effective performance and successful completion of maintenance services.

• Prepare and provide coaching / training to maintenance team to improve personal and professional career development.

3. Reliability (30%)

• Develop and implement reliability strategies to ensure performance and operation efficiency of utility systems maintained well. Conduct routine inspections, troubleshoot issues, and coordinate repairs or upgrades as needed to minimize downtime and maximize efficiency.

• Support Plan and execute scheduled preventive maintenance activities to prevent failures.

• Routinely audit the operational performance and regulatory compliance of systems.

• Ensure all the contractors and vendor / suppliers given proper technical direction with an emphasis on safety, reliability and GMP/GDP.

• Perform work within budget and schedule parameters and provide appropriate feedback to manager for workload, schedule and cost management.

• Perform and/or facilitate on-site startup and training activities.

4. Start-Up and maintenance management for Utility and process equipment system (20%)

• Support and participate in commissioning & qualification of related systems in an operating plant, including related HAZOP, HAZID, FMEA, SOP, CMMS, maintenance procedures and regulation requirements. 

• Participate in system startup, shake down, pre startup check and commissioning of the engineering and process systems.

• Review and update the operation support documents like SOP, PM plan, Training matrix.

5. Cross-functional Collaboration (20%)

• Support investigations and root cause analysis of repetitive problems and investigate equipment failures as part of deviation investigation and CAPA.

• Comply with requirements from Sanofi Safety Program including Health and Safety regulations and OSHA requirements.

• Coordinate with manufacturing and maintenance planner to establish the detailed maintenance plan for the site without impact on production schedule.

• Work closely with other department disciplines, production teams, quality assurance, and regulatory affairs to support the overall objectives of the vaccine manufacturing project. Collaborate on interdisciplinary projects and initiatives to optimize operations and drive continuous improvement.

Qualification and Requirement

• ITE/Diploma in Mechanical/Electrical Engineering from an accredited technical institution.

• Minimum 8/5 years’ experience in utility and single used system operation and maintenance management, preferably with plant operations in engineering field, preferably with pharmaceutical manufacturing experience.

• Added advantage with Boiler Competence certification. Previous experience in utility engineering within the pharmaceutical or biotechnology industry, with specific experience in vaccine manufacturing highly desirable.

• Excellent communication and interpersonal skills, with the ability to collaborate effectively across multidisciplinary teams.

• Commitment to quality, safety, and compliance in all aspects of utility system operation and maintenance.
   

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Job title : QC Support Expert

• Hiring Manager: Quality Control Manager

• Location: Aventis Pharma Manufacturing, Jurong, Singapore

Transform Lives Through Excellence in Quality Control

At Sanofi, we deliver 4.3 billion healthcare solutions to people every year, transforming the practice of medicine through breakthrough science that improves people's lives. Our Manufacturing & Supply teams ensure this impact through flawless planning and meticulous attention to detail. With your expertise in Quality Control, you'll help us protect more people from infectious diseases and bring hope to patients and their families worldwide.
 

Your Impact

As our Quality Control Support Expert, you'll be the cornerstone of laboratory excellence, ensuring compliance, efficiency, and continuous improvement in our quality control operations. Your expertise will directly contribute to patient safety and product quality through:

Key Responsibilities:

Equipment & Systems Management

• Ensure comprehensive lifecycle management of QC laboratory equipment
• Lead qualification and maintenance operations for QC equipment
• Establish metrics and monitor qualification activities to identify trends
• Ensure all QC equipment are properly qualified and maintained
• Serve as SME for Labware LIMS and collaborate with global functions

Technical Leadership & Method Management

• Lead compendial compliance assessment and adherence for the QC laboratory
• Support annual method reviews within the product review framework
• Lead periodic analytical method control trend reviews and recommend improvements
• Support the invalid assay trending program in the QC laboratory
• Participate in Change Control Request facilitation for QC test methods

Digital & Data Management

• Implement and maintain QC digital solutions (core and local models)
• Ensure proper documentation, review, and approval of qualification deliverables
• Record all required data and calculations in compliance with cGMP and Data Integrity requirements
• Provide technical system administrator support for QC GXP computerized systems

Quality & Compliance

• Maintain site validation master plan and procedures related to ALCM and CPV
• Investigate and resolve quality control events promptly
• Provide support during regulatory inspections and audits
• Represent the site in Communities of Practice (CoPs) led by global teams
• Deputize as QC Manager when required

Safety & Continuous Improvement

• Ensure compliance with HSE policies and site procedures
• Embrace Zero Incident Mindset and adhere to Life Saving Rules
• Lead initiatives for continuous improvement in QC support processes
• Practice and communicate laboratory safety standards

What You Bring

• Strong chemistry background with technical expertise in laboratory equipment qualification and analytical method validation
• Experience with LIMS and laboratory computerized systems
• Knowledge of cGMP, data integrity requirements, and regulatory standards
• Excellent problem-solving skills and attention to detail
• Strong communication and collaboration abilities
• Commitment to quality, safety, and continuous improvement

Why Join Us?

Join our team and be part of a mission that matters. At Sanofi, you'll have the opportunity to grow professionally while making a meaningful difference in patients' lives. Your expertise in quality control will directly contribute to our ability to deliver safe, effective healthcare solutions globally.
 

Ready to get started? Apply now and help us chase the miracles of science to improve people's lives.

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Job title: Maintenance Engineer

Location: Singapore

About the Job

Our Team/Overview:

Maintenance Engineer is under the remit of Reliability & Maintenance function, which is part of the Site Engineering & Maintenance organization.

Main Accountabilities:

• Timely execution of preventive/corrective maintenance

• HSE considerations for maintenance (permits, PTW, LOTO)

• WO accuracy and completeness

• Continuous improvement for maintenance operations

Key involvement in Decision Making process

Key roles (A,I):

• I: maintenance plans, procedures, work instructions

• A: shop organization and safety (incl. tools, equipment)

• A: maintainability improvements (accessibility, safety, CI)

• A: feedback to reliability engineering and P&S team

Local specificities

• Develop a maintenance plan in alignment with Failure Modes and Effects Analysis (FMEA) by incorporating risk management strategies and proactive maintenance practices to prevent equipment failures.

• Ability to create preventive and predictive maintenance strategies for manufacturing equipment, ensuring that the maintenance plan aligns with the global maintenance strategy approach.

• Knowledge in setting up an initial inventory of spare parts based on the criticality of equipment and manufacturer recommendations, ensuring smooth plant operations after startup.

• Maintain accurate inventory records and ensure timely replenishment by coordinating with vendors.

• Ensure that all equipment maintenance activities and setups comply with applicable industry regulations such as cGMP, FDA guidelines, and other relevant standards.

• Proficiency in using SAP to track maintenance schedules, manage work orders, maintain spare parts inventories, and record maintenance history.

• Oversee the maintenance, repair, and troubleshooting of key equipment utilized in the manufacturing process.

• Address equipment failures or breakdowns promptly to minimize production downtime and maintain smooth operations.

• Maintain thorough documentation for compliance purposes, including the creation of maintenance plans, work order logs, change requests, deviations, and corrective actions.

• Collaborate closely with production, quality control, and engineering teams to identify equipment issues, suggest solutions, and implement necessary changes.

• Coordinate with vendors and suppliers for maintenance services and spare parts procurement.

• Identify opportunities to optimize processes, reduce costs, and enhance efficiency in relation to equipment and maintenance practices.

• Ensure all maintenance activities are performed safely, adhering to company safety policies, risk assessments, and regulatory requirements.

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Taking care of people is at the heart of everything we do, and we start by taking care of you, our valued colleague. A career at Sedgwick means experiencing our culture of caring. It means having flexibility and time for all the things that are important to you. It's an opportunity to do something meaningful, each and every day. It's having support for your mental, physical, financial and professional needs. It means sharpening your skills and growing your career. And it means working in an environment that celebrates diversity and is fair and inclusive.
A career at Sedgwick is where passion meets purpose to make a positive impact on the world through the people and organizations we serve. If you are someone who is driven to make a difference, who enjoys a challenge and above all, if you're someone who cares, there's a place for you here. Join us and contribute to Sedgwick being a great place to work.
Great Place to Work®
Top 100 Most Loved Workplace®
Forbes Best-in-State Employer
Executive Adjusting Assistant
Working from an office base you will assist the Major Complex Loss Adjusting Team by providing support with the settlement of claims within the terms of the insurance policy.
You will deliver the highest level of customer service by assisting with the management of a portfolio of claims. You should work closely with your manager/team colleagues but will be required to work independently therefore you must be able to work using your own initiative.
Main duties are:
+ Assist Major Complex Loss Team with Report preparation in order to settle claims promptly;
+ Provide administrative support to Major Complex Loss Team;
+ Conduct telephone contact with the insured or and or others in a professional and effective manner;
+ Maintain regular contact with your Adjusting Team to discuss service delivery or to discuss and agree any actions for more complex or challenging claims;
+ Maintain day to day control of your own work level;
+ Comply with Sedgwick processes and procedures;
+ Meet operational targets as agreed with your line manager;
+ Comply with client service standards;
+ Ensure information and data is only disclosed to authorised parties to maintain the confidentiality of information;
+ Achieve objectives as agreed with your line manager during appraisals/one to one meetings;
+ Establish and maintain trust with your colleagues;
+ Strive for continued personal development and growth.
Main requirements of the job holder:
+ Minimum 2 years working experience in the insurance industry;
+ Good oral and written communication;
+ PC literate;
+ Good interpersonal skills;
+ Good attitude and willingness to learn;
+ Ability to interpret policy wordings;
+ Good self-initiative and ability to adapt quickly in different situations;
+ Good time management;
+ Good understanding of Insurance Principles.
Sedgwick is an Equal Opportunity Employer.
The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Sedgwick retains the discretion to add or to change the duties of the position at any time.
**Sedgwick is the world's leading risk and claims administration partner, which helps clients thrive by navigating the unexpected. The company's expertise, combined with the most advanced AI-enabled technology available, sets the standard for solutions in claims administration, loss adjusting, benefits administration, and product recall. With over 33,000 colleagues and 10,000 clients across 80 countries, Sedgwick provides unmatched perspective, caring that counts, and solutions for the rapidly changing and complex risk landscape. For more, see** **sedgwick.com**

Business Development Manager, SEA
Are you an experienced consultative sales professional who loves selling to the Petrochemical industry?
Are you motivated to achieve targets and goals?
About the Business
At ICIS, our mission is to optimize the world's resources. We help companies make strategic, sustainable decisions by bringing transparency to markets across the world. We create a comprehensive view of commodities markets, providing companies with the data and intelligence to successfully navigate across global value chains every day. Our customers benefit from instant access to price assessments, reports and forecasts, a dedicated news channel and supply and demand data. You can learn more about ICIS at the link below. the Role
ICIS is seeking a Business Development Manager to join its business development team in Singapore. Primarily focused on generating business for its petrochemical portfolio with targeted prospects across South East Asia.
Responsibilities
+ Lead business development activities, develops acquisition strategies and plans to win new clients amongst sectors like automotive, fast moving consumer goods, electronics and energy.
+ Responsible for market expansion by acquiring new customers in allocated territories who are interested in a long-term investment in our product and solutions
+ Partners with customers to identify challenges and understand their business needs to establish the best solutions ICIS can provide
+ Navigate prospect organisations to identify and connect with all relevant stakeholders, effectively nurture and maximise opportunities.
+ Experience solution selling, as a consultative approach, focusing on prospect objectives, establishing value, demonstrating return and setting long term relationships.
+ Effectively communicates the value proposition of our products through value-led discussions, demos and proposals.
+ Effectively build, manage, and close a sales pipeline
+ Practice good data management by entering and maintaining customer information into Salesforce.com and relevant CRM databases
Requirements
+ Highly self-motivated, energetic individual who builds strong relationships quickly
+ A natural on the phone, comfortable, to have high in-depth business discussions with senior
+ Great at execution: results driven, detail oriented, organized self-starter
+ Great negotiation and communication skills -able to conduct cold calls effectively
+ Strong focus on solution sales and selling on value with experience in a BDM role
+ Commercially minded with a strong motivation to succeed in a high performing sales team
+ Flexible and adaptable to meet the needs of the changing market, our customers and the business decision makers
Learn more about the LexisNexis Risk team and how we work here ( are committed to providing a fair and accessible hiring process. If you have a disability or other need that requires accommodation or adjustment, please let us know by completing our Applicant Request Support Form or please contact .
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RELX is a global provider of information-based analytics and decision tools for professional and business customers, enabling them to make better decisions, get better results and be more productive.
Our purpose is to benefit society by developing products that help researchers advance scientific knowledge; doctors and nurses improve the lives of patients; lawyers promote the rule of law and achieve justice and fair results for their clients; businesses and governments prevent fraud; consumers access financial services and get fair prices on insurance; and customers learn about markets and complete transactions.
Our purpose guides our actions beyond the products that we develop. It defines us as a company. Every day across RELX our employees are inspired to undertake initiatives that make unique contributions to society and the communities in which we operate.

**Make an impact with NTT DATA**
Join a company that is pushing the boundaries of what is possible. We are renowned for our technical excellence and leading innovations, and for making a difference to our clients and society. Our workplace embraces diversity and inclusion - it's a place where you can grow, belong and thrive.
**Your day at NTT DATA**
The Software Development Engineer is a seasoned subject matter expert, tasked with participating in designing, developing, and testing software systems, modules, or applications for software enhancements and new products including cloud-based or internet-related tools.
This role is accountable for participating in detailed design for certain modules/sub-systems, doing prototype for multi-vendor infrastructure, and showcasing it internally or externally to clients.
This role designs and develops functionality in a micro-services environment working with APIs, telemetry data, and running ML/AI algorithms on it, working with both structured and unstructured data.
**Key responsibilities:**
+ Designs and develops solutions and functionality that drives the growth of business.
+ Accountable for writing and testing code.
+ Accountable for execution of automated testing.
+ Contributes to software deployment.
+ Works across multiple teams to deliver software components while working in collaboration with the product team.
+ Contributes to the integration and building of solutions through automation and coding, using 3rd party software.
+ Creates, crafts and debugs large scale distributed systems.
+ Contributes to writing, updating and maintaining the technical program, end-user documentation, and operational procedures.
+ Accountable for refactoring code.
+ Works across multiple teams to review code written by other developers.
+ Performs any other related task as required.
**To thrive in this role, you need to have:**
+ Excellent understanding of cloud architecture and services in multiple public clouds like AWS, GCP, Microsoft Azure, and Microsoft Office 365.
+ Subject matter expert in programming languages such as C/C++, C#, Java, JavaScript, Python, Node.js, libraries and frameworks.
+ Seasoned expertise of data structures, algorithms, and software design with strong analytical and debugging skills.
+ Seasoned knowledge of micro services-based software architecture and experience with API product development.
+ Seasoned expertise in SQL and no-SQL data stores including Elasticsearch, MongoDB, Cassandra.
+ Seasoned understanding of container run time (Kubernetes, Docker, LXC/LXD).
+ Seasoned proficiency with agile, lean practices and believes in test-driven development.
+ Possess a can-do attitude and one that takes initiative.
+ Excellent ability to work well in a diverse team with different backgrounds and experience levels.
+ Excellent ability to thrive in a dynamic, fast-paced environment.
+ Seasoned proficiency with CI/CD concepts and tools.
+ Seasoned proficiency with cloud-based infrastructure and deployments.
+ Excellent attention to detail.
**Academic qualifications and certifications:**
+ Bachelor's degree or equivalent in Computer Science, Engineering or a related field.
+ Microsoft Certified Azure Fundamentals preferred.
+ Relevant agile certifications preferred.
**Required experience:**
+ Seasoned experience working with geo-distributed teams through innovation, bootstrapping, pilot, and production phases with multiple stakeholders to the highest levels of quality and performance
+ Seasoned experience with tools across full software delivery lifecycle, for example, IDE, source control, CI, test, mocking, work tracking, defect management.
+ Seasoned experience in Agile and Lean methodologies, Continuous Delivery / DevOps, Analytics / data-driven processes.
+ Seasoned proficiency in working with large data sets and ability to apply proper ML/AI algorithms.
+ Seasoned experience in developing micro-services and RESTful APIs.
+ Seasoned experience in software development.
**Workplace type** **:**
On-site Working
**About NTT DATA**
NTT DATA is a $30+ billion trusted global innovator of business and technology services. We serve 75% of the Fortune Global 100 and are committed to helping clients innovate, optimize and transform for long-term success. We invest over $3.6 billion each year in R&D to help organizations and society move confidently and sustainably into the digital future. As a Global Top Employer, we have diverse experts in more than 50 countries and a robust partner ecosystem of established and start-up companies. Our services include business and technology consulting, data and artificial intelligence, industry solutions, as well as the development, implementation and management of applications, infrastructure, and connectivity. We are also one of the leading providers of digital and AI infrastructure in the world. NTT DATA is part of NTT Group and headquartered in Tokyo.
**Equal Opportunity Employer**
NTT DATA is proud to be an Equal Opportunity Employer with a global culture that embraces diversity. We are committed to providing an environment free of unfair discrimination and harassment. We do not discriminate based on age, race, colour, gender, sexual orientation, religion, nationality, disability, pregnancy, marital status, veteran status, or any other protected category. Join our growing global team and accelerate your career with us. Apply today.