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Michael Page Jobs overseas

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Logistics Specialist at Michael Page
North Holland, North Holland, Luxembourg - Full Time
Skills Needed
N/A
Experience Required
Minimum 4 year(s)
Logistics Specialist at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Business Performance / Business Intelligence Analyst at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Compliance Manager / AML at Michael Page
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 10 year(s)
Legal and Compliance Manager (m/f/d) - Financial Service at Michael Page
berlin, Hesse, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 20 year(s)
Senior Brand Manager at Michael Page
England, Cornwall - England, United Kingdom - Full Time
Skills Needed
N/A
Junior Finance Analyst at Michael Page
London, Northamptonshire - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Transport Specialist at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Customer Service Administrator at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
HR Generalist at Michael Page
Dubai, Dubai, United Arab Emirates - 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)
Financial Controller at Michael Page
Victoria, Victoria, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 10 year(s)
Customer Service Advisor at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Senior Finance Analyst at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Senior Finance Manager at Michael Page
Victoria, Victoria, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 10 year(s)
Banking Associate at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Supply Chain Manager at Michael Page
Germany, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Banking Operations at Michael Page
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 8 year(s)
HR Generalist at Michael Page
Dubai, Dubai, United Arab Emirates - 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)
Management Accountant at Michael Page
Victoria, Victoria, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 10 year(s)
IT-Security Administrator (m/w/d) at Michael Page
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Logistics Specialist at Michael Page
North Holland, North Holland, Luxembourg -
Full Time

Start Date

Immediate

Expiry Date

31 Jan, 27

Salary

50000.0

Posted On

02 Nov, 26

Experience

4 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Industry

Transportation & Logistics

Description

Les entreprises et les gouvernements comptent sur Thales pour apporter de la confiance aux milliards d’interactions numériques qu’ils établissent avec les utilisateurs. L’Activité Mondiale Identité & Sécurité Numériques (DIS) fournit des technologies et services (des logiciels sécurisés en passant par la biométrie ou encore le cryptage), qui permettent aux entreprises ainsi qu’aux gouvernements de vérifier des identités, et de protéger les données afin qu’elles restent sûres.Order & Billing Specialist

The Order & Billing Specialist is the central point of the customer order process, managing the full operational flow from signed offer to customer invoicing. The role covers order setup, billing of consultant hours, supplier purchase orders, delivery follow-up and customer billing, while coordinating with multiple teams and systems. Strong multitasking, organization, autonomy, and attention to detail are essential.


Responsibilities

  • Check and set up contracts in the system.
  • Prepare and issue accurate client invoices in a timely manner.
  • Collaborate with the sales and finance teams to ensure timely month-end and year-end closing.
  • Process purchase orders and ensure the timely acquisition of goods and services.
  • Manage activities across multiple systems and complex processes, ensuring accurate and timely execution.
  • Resolve client queries related to billing and deliveries of goods and services.


Qualifications and Skills:

  • Proven experience in billing, order management, purchasing or a related administrative role.
  • Solid understanding of billing and purchasing processes.
  • Comfortable working with multiple and complex systems, tools, and processes.
  • Strong organizational and problem-solving skills, with excellent attention to detail.
  • Resilience, adaptability, and a strong ability to find practical solutions in a complex operational environment.
  • Strong follow-up and communication skills.
  • English: B2 or above
  • French : Fluent


Thales, entreprise Handi-Engagée, reconnait tous les talents. La diversité est notre meilleur atout. Postulez et rejoignez nous

How To Apply:

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Responsibilities
Logistics Specialist at Michael Page
North Holland, North Holland, Luxembourg - Full Time
Skills Needed
N/A
Experience Required
Minimum 4 year(s)
Logistics Specialist at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Business Performance / Business Intelligence Analyst at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Compliance Manager / AML at Michael Page
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 10 year(s)
Legal and Compliance Manager (m/f/d) - Financial Service at Michael Page
berlin, Hesse, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 20 year(s)
Senior Brand Manager at Michael Page
England, Cornwall - England, United Kingdom - Full Time
Skills Needed
N/A
Junior Finance Analyst at Michael Page
London, Northamptonshire - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Transport Specialist at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Customer Service Administrator at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
HR Generalist at Michael Page
Dubai, Dubai, United Arab Emirates - 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)
Financial Controller at Michael Page
Victoria, Victoria, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 10 year(s)
Customer Service Advisor at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Senior Finance Analyst at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Senior Finance Manager at Michael Page
Victoria, Victoria, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 10 year(s)
Banking Associate at Michael Page
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Supply Chain Manager at Michael Page
Germany, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Banking Operations at Michael Page
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 8 year(s)
HR Generalist at Michael Page
Dubai, Dubai, United Arab Emirates - 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)
Management Accountant at Michael Page
Victoria, Victoria, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 10 year(s)
IT-Security Administrator (m/w/d) at Michael Page
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A