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Principal Business Analyst - Workforce Mobility Project at Kingston Human Capital
Australia, Massachusetts, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Senior Business Analyst at Kingston Human Capital
Australia, Massachusetts, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Comptable Unique at Toronto Humane Society
Paris, Franche Comte, France - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Principal Business Analyst - Workforce Mobility Project at Kingston Human Capital
Australia, Massachusetts, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Enterprise Architect at Kingston Human Capital
Australia, Alberta, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 10 year(s)
Enterprise Architect at Kingston Human Capital
Western Australia, Western Australia, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 20 year(s)
Customer Service Representative ( at HumanOptics Holding AG
berlin, Berlin, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 17 year(s)
Manager - Financial Planning at Human Rights Watch HRW
Sydney, South Australia, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 12 year(s)
Customer Service Representative (m/f/d) at HumanOptics Holding AG
Ireland, Dundee - Scotland, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Financial Planning Manager at Human Rights Watch HRW
Sydney, South Australia, Australia - Full Time
Skills Needed
N/A
Project Lead at Kingston Human Capital
Sydney, South Australia, Australia - Full Time
Skills Needed
N/A
Civil Engineer at Kingston Human Capital
Victoria, Queensland, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 6 year(s)
Regulatory Affairs Specialist (m/f/d) at HumanOptics Holding AG
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Regulatory Affairs Specialist (M/W/D) IHRE AUFGABEN · Zulassung at HumanOptics Holding AG
Berlin, Berlin, Germany - 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 12 year(s)
REGULATORY AFFAIRS SPECIALIST at HumanOptics Holding AG
Berlin, Berlin, Germany - 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 12 year(s)
Behaviour & Animal Care Support Associate - Full Time at Calgary Humane Society
Ontario, Ontario, Canada - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
MTLA oder Biologe (m/w/d) für Humangenetik (Vollzeit) at Eurofins Germany
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Business Development Manager Humanoid Robotics (m/w/d) at Brose
Germany, Alberta, Germany - Full Time
Skills Needed
N/A
Senior Specialist, Human Capital Strategy & Projects at Tamworth M42 Travelodge
Dubai, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Experience Required
Minimum 15 year(s)
Senior Specialist, Human Capital Strategy & Projects at LinkedIn
Dubai, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Experience Required
Minimum 7 year(s)
Principal Business Analyst - Workforce Mobility Project at Kingston Human Capital
Australia, Massachusetts, Australia -
Full Time

Start Date

Immediate

Expiry Date

10 Nov, 26

Salary

150000.0

Posted On

27 Oct, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Industry

Information Technology & Services

Description

How To Apply:

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

Responsibilities
Principal Business Analyst - Workforce Mobility Project at Kingston Human Capital
Australia, Massachusetts, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Senior Business Analyst at Kingston Human Capital
Australia, Massachusetts, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Comptable Unique at Toronto Humane Society
Paris, Franche Comte, France - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Principal Business Analyst - Workforce Mobility Project at Kingston Human Capital
Australia, Massachusetts, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Enterprise Architect at Kingston Human Capital
Australia, Alberta, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 10 year(s)
Enterprise Architect at Kingston Human Capital
Western Australia, Western Australia, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 20 year(s)
Customer Service Representative ( at HumanOptics Holding AG
berlin, Berlin, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 17 year(s)
Manager - Financial Planning at Human Rights Watch HRW
Sydney, South Australia, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 12 year(s)
Customer Service Representative (m/f/d) at HumanOptics Holding AG
Ireland, Dundee - Scotland, Germany - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Financial Planning Manager at Human Rights Watch HRW
Sydney, South Australia, Australia - Full Time
Skills Needed
N/A
Project Lead at Kingston Human Capital
Sydney, South Australia, Australia - Full Time
Skills Needed
N/A
Civil Engineer at Kingston Human Capital
Victoria, Queensland, Australia - Full Time
Skills Needed
N/A
Experience Required
Minimum 6 year(s)
Regulatory Affairs Specialist (m/f/d) at HumanOptics Holding AG
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Regulatory Affairs Specialist (M/W/D) IHRE AUFGABEN · Zulassung at HumanOptics Holding AG
Berlin, Berlin, Germany - 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 12 year(s)
REGULATORY AFFAIRS SPECIALIST at HumanOptics Holding AG
Berlin, Berlin, Germany - 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 12 year(s)
Behaviour & Animal Care Support Associate - Full Time at Calgary Humane Society
Ontario, Ontario, Canada - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
MTLA oder Biologe (m/w/d) für Humangenetik (Vollzeit) at Eurofins Germany
Berlin, Berlin, Germany - Full Time
Skills Needed
N/A
Business Development Manager Humanoid Robotics (m/w/d) at Brose
Germany, Alberta, Germany - Full Time
Skills Needed
N/A
Senior Specialist, Human Capital Strategy & Projects at Tamworth M42 Travelodge
Dubai, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Experience Required
Minimum 15 year(s)
Senior Specialist, Human Capital Strategy & Projects at LinkedIn
Dubai, Dubai, United Arab Emirates - Full Time
Skills Needed
N/A
Experience Required
Minimum 7 year(s)