Regulatory Affairs Consultant
Location: SwitzerlandSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Medical Devices organization, based in Genf Switzerland.
Medical Device company with a very innovative portfolio of Class III devices (Infiltration syringes and tubes).
ROLE DESCRIPTION
Due to a letter from the notified bodies, the company needs to update their Regulatory DHF history file.
Other relevant information:
- Starting date: ASAP (it is urgent)
- Availability: full-time
- Work remotely: 1 - 2 days are required to be on site
- Duration: 3-6 months (the project is for 1 specific file)
RESPONSIBILITIES
- Update/ Modify the Regulatory DHF history file
- Support in the certification of the CE Marking
- Revise the clinical studies and evaluations
- Writing the clinical/ regulatory file
- Support the team in the communications with the notified bodies
REQUIREMENTS
- Strong scientific background
- +5 years of relevant working experience in Regulatory Affairs in Medical Devices
- Ability to work independently without much supervision
- Preferably experience with plasma products
- Language skills: English (French appreciated)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.
Opis stanowiska
SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Medical Devices organization, based in Genf Switzerland.
Medical Device company with a very innovative portfolio of Class III devices (Infiltration syringes and tubes).
ROLE DESCRIPTION
Due to a letter from the notified bodies, the company needs to update their Regulatory DHF history file.
Other relevant information:
- Starting date: ASAP (it is urgent)
- Availability: full-time
- Work remotely: 1 - 2 days are required to be on site
- Duration: 3-6 months (the project is for 1 specific file)
RESPONSIBILITIES
- Update/ Modify the Regulatory DHF history file
- Support in the certification of the CE Marking
- Revise the clinical studies and evaluations
- Writing the clinical/ regulatory file
- Support the team in the communications with the notified bodies
REQUIREMENTS
- Strong scientific background
- +5 years of relevant working experience in Regulatory Affairs in Medical Devices
- Ability to work independently without much supervision
- Preferably experience with plasma products
- Language skills: English (French appreciated)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.
Dodatkowe informacje
- Ostatnia aktualizacja
- Wymiar etatu
- Pełny etat
- Rodzaj umowy
- Własna działalność
- Liczba wakatów
- 1
- Min. doświadczenie
- 2 lata
- Min. wykształcenie
- Wyższe licencjackie
- Branża / kategoria
- Praca Badania / Rozwój
