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HR Operations Specialist at Tata Technologies
London England, London - England, United Kingdom - Full Time
Skills Needed
N/A
Retails Operations Manager at Michael Page
Dubai, Abu az Zuluf, United Arab Emirates - Full Time
Skills Needed
N/A
Data Engineer at OSL Retail Services Inc
Victoria, Victoria, Australia - Full Time
Skills Needed
N/A
Data Scientist at SoTalent
Utrecht, Utah, Netherlands - Full Time
Skills Needed
N/A
Talent Acquisition Partner at Independence Australia Group
Victoria, Victoria, Australia - 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)
Senior Talent Acquisition Advisor at CIMIC
Victoria, Victoria, Australia - 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)
Talent Acquisition Partner at Metrea
Victoria, Victoria, Australia - 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)
Talent Acquisition at Charterhouse Group
Victoria, Victoria, Australia - 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)
Recruitment Coordinator at HAYS
Victoria, Victoria, Australia - 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)
Senior Recruitment Consultant at Xclusive Recruitment
Victoria, Victoria, Australia - 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)
Software Development Engineer in Test at Humand
Limburg, Limburg, Ireland - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Learning Support Assistant at MILK EDUCATION
Dubai, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Civil Supervisor at Norbar Torque Tools Inc
Victoria, Queensland, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 3 year(s)
Sales And Business Development at Barrhead Fastfood Limited t/a Jewels of Asia
England, London - England, United Arab Emirates - Full Time
Skills Needed
N/A
Experience Required
Minimum 3 year(s)
Marketing Manager at Global Community Charter School GCCS
dublin, Dublin County, Ireland - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Clinical Trial Assistant 2 at LinkedIn
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Financial Controller at VM Drilling PTY LTD
Victoria, Victoria, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 10 year(s)
Assistant Warehouse Manager at Kumho Tyre Australia Pty Ltd
victoria, New South Wales, Australia - Full Time
Skills Needed
N/A
Operator chemische Produktion (m/w/d) at adesta GmbH Co KG
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Buyer at JENATEC Industriemontagen GmbH Berlin
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
HR Operations Specialist at Tata Technologies
London England, London - England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

18 Nov, 26

Salary

0.0

Posted On

20 Aug, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Information Services

Description

The Role:

We’re looking for a proactive, highly organised HR Operations Specialist/Coorindator to join our UK HR team. If you have HR experience, a drive to develop, and a passion for improving how things work, this role offers a great opportunity to grow within a supportive HR function. You’ll play a key role in day‑to‑day HR operations, including visa coordination, responding to HR queries, managing benefits engagement, maintaining employee records, supporting exit interviews, and contributing to employee engagement and recognition activities.

 

Area of Responsibility  

 

·        Be the go‑to HR contact, offering friendly and timely support to employees, resolving queries where you can, and escalating where topics need specialist attention.

·        Visa & Right‑to‑Work coordination—keeping processes on track, managing applications, renewals and compliance checks, communicating clearly with employees, and using your initiative to spot and flag potential issues early

·        Support our benefits programme—co‑ordinating processes, managing benefits for starters and leavers, liaising with providers, assisting employees with queries, and arranging engaging benefits sessions

·        Help bring our culture to life—co‑ordinating long‑service awards, recognition activities, employee events, communications, and supporting actions from survey feedback

·        Coordinate smooth offboarding experiences, conduct exit interviews, and spot trends that help shape ongoing improvements.

·        Employee file management—keeping records up to date, organised, and fully compliant with documentation requirements

As the role grows, you’ll have the opportunity to develop your skills in areas such as Employee Relations casework, HR project support, and continuous improvement initiatives.

 

Knowledge / Experience

 

·        Previous HR experience as an HR Administrator/Advisor/Coordinator who is comfortable with operational tasks as well as supporting on HR related projects.

·        Strong organisational skills with excellent attention to detail

·        Proactive approach, with a desire to improve processes and ways of working as you go

·        Ability to manage multiple priorities in a fast‑paced environment

·        Excellent communication skills and ability to handle sensitive information

·        Experience with the Home Office Sponsor Management System (SMS) would be an advantage.

  • ·        An interest in expanding your knowledge and career in HR

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities
HR Operations Specialist at Tata Technologies
London England, London - England, United Kingdom - Full Time
Skills Needed
N/A
Retails Operations Manager at Michael Page
Dubai, Abu az Zuluf, United Arab Emirates - Full Time
Skills Needed
N/A
Data Engineer at OSL Retail Services Inc
Victoria, Victoria, Australia - Full Time
Skills Needed
N/A
Data Scientist at SoTalent
Utrecht, Utah, Netherlands - Full Time
Skills Needed
N/A
Talent Acquisition Partner at Independence Australia Group
Victoria, Victoria, Australia - 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)
Senior Talent Acquisition Advisor at CIMIC
Victoria, Victoria, Australia - 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)
Talent Acquisition Partner at Metrea
Victoria, Victoria, Australia - 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)
Talent Acquisition at Charterhouse Group
Victoria, Victoria, Australia - 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)
Recruitment Coordinator at HAYS
Victoria, Victoria, Australia - 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)
Senior Recruitment Consultant at Xclusive Recruitment
Victoria, Victoria, Australia - 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)
Software Development Engineer in Test at Humand
Limburg, Limburg, Ireland - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Learning Support Assistant at MILK EDUCATION
Dubai, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Civil Supervisor at Norbar Torque Tools Inc
Victoria, Queensland, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 3 year(s)
Sales And Business Development at Barrhead Fastfood Limited t/a Jewels of Asia
England, London - England, United Arab Emirates - Full Time
Skills Needed
N/A
Experience Required
Minimum 3 year(s)
Marketing Manager at Global Community Charter School GCCS
dublin, Dublin County, Ireland - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Clinical Trial Assistant 2 at LinkedIn
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Financial Controller at VM Drilling PTY LTD
Victoria, Victoria, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 10 year(s)
Assistant Warehouse Manager at Kumho Tyre Australia Pty Ltd
victoria, New South Wales, Australia - Full Time
Skills Needed
N/A
Operator chemische Produktion (m/w/d) at adesta GmbH Co KG
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Buyer at JENATEC Industriemontagen GmbH Berlin
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A

Frequently Asked Questions

You can get a job abroad from India by following a clear, step-by-step process:

  1. Identify your target country and check its visa and job requirements.
  2. Prepare a globally accepted resume and cover letter that highlight your skills.
  3. Apply through trusted job portals or directly on company career pages.
  4. Work only with licensed overseas recruiters approved by the Indian government.
  5. Obtain the correct work visa before relocation.

The best job abroad depends on your skills, education, and career goals. In 2025, roles in Information Technology, Healthcare, Engineering, Finance, and Skilled Trades are among the most in demand worldwide. These fields offer strong growth potential, high salaries, and visa sponsorship options in many countries.

Yes, freshers can get jobs abroad. Countries such as Germany and Japan offer entry-level or training programs for young professionals through vocational training or specified skilled worker routes. The UAE and other Gulf countries also have entry-level positions in hospitality, retail, and customer service. Building global certifications, language skills, and a professional resume increases your chances.

Globally, the most in-demand jobs in 2025 include:

  • IT and Data Roles – Software Engineers, Data Scientists, Cybersecurity Experts
  • Healthcare Roles – Nurses, Medical Technicians, Physiotherapists
  • Engineering Roles – Civil, Mechanical, and Electrical Engineers
  • Finance and Accounting – Auditors, Financial Analysts, Accountants
  • Skilled Trades – Welders, Electricians, HVAC Technicians

These occupations face consistent global talent shortages and are prioritized for visa sponsorship in many countries.

Current overseas job openings for Indian citizens can be found on recognized international job platforms, professional networking sites, and verified recruitment agencies. You can also explore official government resources that list approved overseas employers and recruiters. Always verify the authenticity of job offers and avoid sharing personal or financial information with unverified sources.

Yes, there is a continuous global demand for engineers across multiple sectors. Opportunities exist for civil, mechanical, electrical, and software engineers in countries with growing infrastructure, technology, and energy projects. To qualify, you generally need a recognized engineering degree, relevant work experience, professional certifications, and—where required—language proficiency or licensing from the destination country.
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