Regulatory/Scientific Support in NA4, ECHA, Helsi

at  StaffPoint Oy

Helsinki, Etelä-Suomi, Finland -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate05 Aug, 2024Not Specified06 May, 2024N/ATeamwork,Interpersonal Skills,EnglishNoNo
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Description:

We are looking for a full-time interim for Regulatory/Scientific Support for a temporary 4 months project together with our client European Chemicals Agency ECHA. Please note that the working language is English. The job starts 1.6.2024 and it ends 30.9.2024.
General description:
The Regulatory / Scientific administrative support staff member will assist the Data validation and completeness team in the tasks related to the scientific and operational activities of the European Chemicals Agency (ECHA). In particular, they will work in the area of the completeness check of REACH registration data and contribute to the activities to improve data availability for the Agency’s processes.

Duties:

  • Perform checks on registration dossiers according to Article 20(2) of REACH to ensure that the administrative and scientific data provided by registrants is complete according to the REACH provisions.
  • Carry out administrative tasks to process the dossiers and document the decisions in the relevant system.
  • Continuously develop expertise in assessing regulatory and scientific information against defined criteria.
  • Support the further development and testing of the IUCLID data validation rules.
  • Provide company support by drafting answers to Helpdesk questions and placing company calls.

We excpect from you / requirements:

  • Experience in assessing content of administrative, technical or scientific nature following written instructions and strict deadlines; an eye for details
  • Experience in customer support/interaction
  • Ability to communicate effectively in written and spoken English
  • Proficiency in using MS Office tools and aptitude to learn new IT applications
  • Ability to complete assigned tasks independently in a timely manner and with little direction
  • Sense of initiative and flexibility
  • Aptitude for teamwork and sharing information
  • Strong interpersonal skills
  • Minimum of one (1) year of professional experience, relevant to the job

Assets for this position:

  • Education in a scientific discipline, e.g., environmental sciences, chemical engineering, pharmacy, IT, etc.
  • Knowledge in chemicals regulations
  • Experience or interest in the development and testing of the IT tools

We offer you:

  • Interesting project in a multicultural environment
  • Versatile tasks and great team support
  • Comprehensive induction

Instructions and additional information:
We will be contacting applicants during application period, hence do not hesitate to leave your CV for the position today! The latest day to leave your application is Sunday 5th May. Please note, that we cannot accept applications via email due to GDPR regulations. All applications must be submitted through StaffPoint’s website.
Please be prepared to tell us two references.
Please note that prior to appointment, successful applicant will be asked to produce an official document indicating that they do not have a criminal record.
Please leave your application and CV in Europass format:
https://europass.cedefop.europa.eu/editors/en/cv/compose
Yhteystiedot: Sanna Apiainen
Recruitment Consultant
[email protected]
Työpaikan osoite: 00150 Helsinki
Palkkaus: According to agreement
Työ alkaa: 01.06.2024
Työaika: Kokoaikatyö
Työn kesto: Määräaikainen
Hakuaika päättyy: 05.05.2024 20:59
Jätä hakemus: https://tyomarkkinatori.fi/henkiloasiakkaat/avoimet-tyopaikat/04d55893-9…
Ilmoitus jätetty: 03.05.2024 11:22
Työmarkkinatorin ilmoitusnumero: 04d55893-9c01-4d29-af19-7c22f4a69e4a
Lähde: Työmarkkinatorin asiakastietojärjestelmä
.
StaffPoint Oy
Helsinki
Uusimaa
Kokopäiväinen, Määräaikainen ja projektityö
Julkaistu 03.05.202

How To Apply:

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

Responsibilities:

  • Perform checks on registration dossiers according to Article 20(2) of REACH to ensure that the administrative and scientific data provided by registrants is complete according to the REACH provisions.
  • Carry out administrative tasks to process the dossiers and document the decisions in the relevant system.
  • Continuously develop expertise in assessing regulatory and scientific information against defined criteria.
  • Support the further development and testing of the IUCLID data validation rules.
  • Provide company support by drafting answers to Helpdesk questions and placing company calls


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Information Technology/IT

Pharma / Biotech / Healthcare / Medical / R&D

Other

Graduate

Proficient

1

Helsinki, Finland