Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
CH - Regulatory Professional - Normal-19927
Eingestellt von Experis Schweiz AG
Gesuchte Skills: Elan, Client
Projektbeschreibung
INTERNATIONAL REGULATORY AFFAIRS MANAGER/MEDICAL DEVICES
On behalf of our client, an international and global company, specialized in medical devices based in Solothurn area, we are looking for an INTERNATIONAL REGULATORY AFFAIRS MANAGER. This is a long contracting position starting AUGUST 2015 until MARCH 2016.
As an INTERNATIONAL REGULATORY AFFAIRS MANAGER you have the chance to provide a compilation of all DOCUMENTATION required for products REGISTRATION in INTERNATIONAL COUNTRIES. You also will determine the STRATEGIES and DEVELOP SOLUTIONS according the internal guidelines. You will manage the work processes and interact with team members, regional resources and Operating Company leadership to oversee the regulatory aspects of the new products launches and control the submission of license application.
IN ORDER TO GIVE THE BEST OUTPUT FOR THE ROLE YOU SHOULD BRING:
- Over 4 years' experience in a similar position
- Relevant experience in the MEDICAL DEVICES sector, expertise in the major regulatory systems (FDA, PMDA etc.)
- Strong stakeholder management and communications skills
- Good analytical skills and strong problem solving ability
- Fluent in (SWISS) GERMAN and ENGLISH
If you are an energetic, independent and a highly motivated individual, currently looking for a challenging new position to apply your skills in a dynamic and well known medical devices' environment with very attractive salary, then we look forward to receiving your application!
I am looking forward to hearing from you!
Probably you know Experis as Elan IT - we have a new name now but we still have the same expertise in IT Recruitment. We are part of the Manpower group and at Experis IT we are responsible for recruitment of the best IT Specialists.
On behalf of our client, an international and global company, specialized in medical devices based in Solothurn area, we are looking for an INTERNATIONAL REGULATORY AFFAIRS MANAGER. This is a long contracting position starting AUGUST 2015 until MARCH 2016.
As an INTERNATIONAL REGULATORY AFFAIRS MANAGER you have the chance to provide a compilation of all DOCUMENTATION required for products REGISTRATION in INTERNATIONAL COUNTRIES. You also will determine the STRATEGIES and DEVELOP SOLUTIONS according the internal guidelines. You will manage the work processes and interact with team members, regional resources and Operating Company leadership to oversee the regulatory aspects of the new products launches and control the submission of license application.
IN ORDER TO GIVE THE BEST OUTPUT FOR THE ROLE YOU SHOULD BRING:
- Over 4 years' experience in a similar position
- Relevant experience in the MEDICAL DEVICES sector, expertise in the major regulatory systems (FDA, PMDA etc.)
- Strong stakeholder management and communications skills
- Good analytical skills and strong problem solving ability
- Fluent in (SWISS) GERMAN and ENGLISH
If you are an energetic, independent and a highly motivated individual, currently looking for a challenging new position to apply your skills in a dynamic and well known medical devices' environment with very attractive salary, then we look forward to receiving your application!
I am looking forward to hearing from you!
Probably you know Experis as Elan IT - we have a new name now but we still have the same expertise in IT Recruitment. We are part of the Manpower group and at Experis IT we are responsible for recruitment of the best IT Specialists.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung