ITOT Site Support

Appealing Points:

• Work on advanced OT and automation systems in a GMP-regulated pharmaceutical manufacturing environment.
• Gain hands-on experience with SCADA, industrial control systems, network infrastructure, and IT/OT integration projects.
• Play a key role in site operations, continuous improvement initiatives, and technology upgrades that directly impact production reliability and efficiency.

Annual salary: 6 million and above

Job Responsibilities:

• The Site ITOT Site Support Role is responsible for the configuration and maintenance of OT relevant computing hardware such as workstations, switches, virtual machines and displays.
• Systems at the Millburn RLT site include plant wide SCADA, 3rd Party Skid and standard-along control systems including freezers, air handlers, chillers and building management systems.
• Collaborate with cross-functional teams to ensure smooth integration of IT and Automation systems.
• Participate in the development and execution of IT and Automation projects.
• Support 24x7 Site operations after start up
• Schedule and perform routine maintenance and upgrades on IT hardware and software.
• Develop and maintain documentation for OT Hardware systems configurations and standard procedures (SOPs), User Requirements (URS), Functional Specifications (FS) and Design Specifications(DDS/HDS/SDS).
• Assist in the implementation of security measures and protocols to protect IT and automation systems.
• Setup and configure hardware that support OT Industrial Control systems including but not limited to network devices, switches, servers, and workstations in a GMP Pharma environment.
• Provide technical support and troubleshooting for IT and automation systems.
• Coordinate with vendors and external partners to resolve any technical issues or procure necessary equipment.
• Participate in Operational Excellence and continuous improvement efforts

Job Qualification:

• Bachelor's degree in Computer Science, Information Technology, automation, engineering or a related field.
• Minimum of 5 years of experience in IT or Automation, in a GMP Pharma environment.
• Strong knowledge of networking protocols, hardware, and troubleshooting.
• Experience in project management for IT or Automation projects
• Experience with setting up and configuring network devices, switches, servers, and workstations.
• Familiarity with automation systems and their integration with IT infrastructure.
• Experience of GMP including 21 CFR 11 regulations and compliance requirements.
• Excellent problem-solving and analytical skills.
• Strong communication and collaboration abilities.
• Ability to work independently and handle multiple tasks simultaneously.
• Certifications such as CCNA, MCSE, or CompTIA A+ are a plus.

Language Skills: Business level Japanese (JLPT N2) and Business level English

Company Description:

One of the world's leading professional services companies, transforming clients' business, operating and technology models for the digital era.

Their unique industry-based, consultative approach helps clients envision, build and run more innovative and efficient businesses.

Headquartered in the U.S., this company is one of the Fortune 500 companies and is consistently listed among the most admired companies in the world.

[Passive smoking measures]

Indoor smoking

Designated smoking area

. Skillset Required: OT relevant computing hardware configuration, maintenance, SCADA, industrial control systems, network infrastructure, IT/OT integration, 24x7 Site operations support, routine maintenance and upgrades on IT hardware and software, documentation development and maintenance, SOPs