Aarorn Technologies Inc Jobs overseas

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Commissioning Engineer at DATAVANT INC
Oslo, Gauteng, Norway - Full Time
Skills Needed
N/A
Junior Designer at Weusthem Inc
Ontario, Ontario, Canada - Full Time
Skills Needed
N/A
Hardware/Test Automation Engineer at V2Soft, Inc.
Toronto, Ontario, Canada - Full Time
Skills Needed
N/A
PMO Manager at Ametek, Inc.
Toronto, Mississippi, Canada - Full Time
Skills Needed
N/A
Experience Required
Minimum 11 year(s)
Sales Coordinator at Accorder Inc
United Arab Emirates, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Experience Required
Minimum 6 year(s)
Project Manager at Gotion, Inc.
Dubai, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Experience Required
Minimum 20 year(s)
Sales & Distribution Director at Virtucom Inc
Dubai, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Project Manager at Gotion, Inc.
Dubai, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Regional Sales Manager at ATRICURE INC
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 9 year(s)
Senior AML Officer (m/f/d) at Fiserv, Inc.
berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 19 year(s)
Technical Business Analyst at Compugen Inc
Toronto, Ontario, Canada - Full Time
Skills Needed
N/A
Experience Required
Minimum 4 year(s)
Clinical Data Manager at CALYSTA INC.
London, Cumbria - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Sales Executive at INCOS STAMPI
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Specialization
As an innovative and internationally oriented manufacturer of premium implants for eye surgery, we develop, produce and distribute medical devices to restore the best possible vision to the human eye. To strengthen our team at our Erlangen location, we are looking for a full-time employee to start as soon as possible. Regulatory Affairs Specialist (M/F/D) YOUR TASKS Approval and registration of medical devices in national and international markets • Preparation of documents for authentication and legalization • Support in maintaining and collaborating on the creation of technical product documentation, including risk management files and regulatory documents within the framework of international regulatory strategies. Project support for implementing the requirements of the new EU Medical Device Regulation and support in maintaining the corresponding approvals. • Internal contact person and contact person for business partners regarding regulatory issues • Regulatory assessment of product and document changes relevant to approval • Support in revising and creating RA-relevant QM documents • Support in ensuring compliance with all guidelines, laws, standards and country-specific requirements • Research of guidelines and laws • Close internal communication and coordination with other departments
Experience Required
Minimum 11 year(s)
Graduate Personal Assistant / Accounts Assistant at Austonia Inc
Sydney, New South Wales, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Senior Test Automation Engineer/Software Development Engineer in Test (d/f/m) at LEAPSOME INC
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Senior Engineer, Chemical Process Engineering at ENTEGRIS INC
Sydney, Western Australia, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 8 year(s)
Lead Software Engineer (m/f/d) at Fincite Gmbh
berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Lead Software Engineer (m/w/d) at Fincite Gmbh
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Lead Software Engineer (m/f/d) at Novanta Inc.
berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 18 year(s)
Pega Lead Developer at Infosoft INC
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 12 year(s)
Commissioning Engineer at DATAVANT INC
Oslo, Gauteng, Norway -
Full Time


Start Date

Immediate

Expiry Date

17 Nov, 26

Salary

0.0

Posted On

19 Aug, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Industry

Oil & Gas

Description

Responsibilities


You will oversee all the commissioning related activities for data center construction projects. This role is essential in ensuring that projects meet the required standards, codes, and regulations. You will work closely with the project teams and EPC contractor, subcontractors and Commissioning Agent to ensure that the project commissioning activities are on Track and quality of work aligns with the company’s expectations and industry best practices.


  • Develop and implement comprehensive commissioning plans for Data Center projects.
  • Define commissioning processes, procedures, and standards.
  • Coordinate with project stakeholders to establish commissioning schedules.
  • Review EPC’s commissioning plan
  • Support in Project set up in Cx Software and manage the project tool
  • Review design specifications and engineering drawings to ensure compliance with commissioning requirements.
  • Conduct detailed reviews of systems including electrical, mechanical, HVAC, and IT infrastructure.
  • Ensure all systems are installed and function as intended.
  • Develop and execute test plans for all data center systems.
  • Supervise and perform functional performance tests, integrated systems testing, and reliability tests.
  • Witness tests and review/approve testing and commissioning reports/filled scripts
  • Monitor the testing and commissioning testing record and report in CX software.

Experience & Qualifications


  • Bachelor’s degree in electrical engineering, Mechanical Engineering, or a related field. Advanced degrees or certifications in commissioning or project management are a plus.
  • 8+ years of experience in commissioning with 4 years of experience in data centre.
  • Experience of Hyperscaler Commissioning process is preferred

Responsibilities
Commissioning Engineer at DATAVANT INC
Oslo, Gauteng, Norway - Full Time
Skills Needed
N/A
Junior Designer at Weusthem Inc
Ontario, Ontario, Canada - Full Time
Skills Needed
N/A
Hardware/Test Automation Engineer at V2Soft, Inc.
Toronto, Ontario, Canada - Full Time
Skills Needed
N/A
PMO Manager at Ametek, Inc.
Toronto, Mississippi, Canada - Full Time
Skills Needed
N/A
Experience Required
Minimum 11 year(s)
Sales Coordinator at Accorder Inc
United Arab Emirates, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Experience Required
Minimum 6 year(s)
Project Manager at Gotion, Inc.
Dubai, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Experience Required
Minimum 20 year(s)
Sales & Distribution Director at Virtucom Inc
Dubai, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Project Manager at Gotion, Inc.
Dubai, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Regional Sales Manager at ATRICURE INC
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 9 year(s)
Senior AML Officer (m/f/d) at Fiserv, Inc.
berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 19 year(s)
Technical Business Analyst at Compugen Inc
Toronto, Ontario, Canada - Full Time
Skills Needed
N/A
Experience Required
Minimum 4 year(s)
Clinical Data Manager at CALYSTA INC.
London, Cumbria - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Sales Executive at INCOS STAMPI
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Specialization
As an innovative and internationally oriented manufacturer of premium implants for eye surgery, we develop, produce and distribute medical devices to restore the best possible vision to the human eye. To strengthen our team at our Erlangen location, we are looking for a full-time employee to start as soon as possible. Regulatory Affairs Specialist (M/F/D) YOUR TASKS Approval and registration of medical devices in national and international markets • Preparation of documents for authentication and legalization • Support in maintaining and collaborating on the creation of technical product documentation, including risk management files and regulatory documents within the framework of international regulatory strategies. Project support for implementing the requirements of the new EU Medical Device Regulation and support in maintaining the corresponding approvals. • Internal contact person and contact person for business partners regarding regulatory issues • Regulatory assessment of product and document changes relevant to approval • Support in revising and creating RA-relevant QM documents • Support in ensuring compliance with all guidelines, laws, standards and country-specific requirements • Research of guidelines and laws • Close internal communication and coordination with other departments
Experience Required
Minimum 11 year(s)
Graduate Personal Assistant / Accounts Assistant at Austonia Inc
Sydney, New South Wales, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Senior Test Automation Engineer/Software Development Engineer in Test (d/f/m) at LEAPSOME INC
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Senior Engineer, Chemical Process Engineering at ENTEGRIS INC
Sydney, Western Australia, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 8 year(s)
Lead Software Engineer (m/f/d) at Fincite Gmbh
berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Lead Software Engineer (m/w/d) at Fincite Gmbh
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Lead Software Engineer (m/f/d) at Novanta Inc.
berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 18 year(s)
Pega Lead Developer at Infosoft INC
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 12 year(s)
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