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Regulatory Affairs Administrator

Uvod o radnom mjestu

Hvala vam na interesu za naš natječaj. Veseli nas što želite saznati više o Dechra Pharmaceuticals PLC.

Dechra je rastuća globalna kompanija koja je specijalizirana za veterinarske lijekove. Stručnjaci smo za razvoj, proizvodnju, marketing i prodaju proizvoda visoke kvalitete koje koriste veterinari diljem svijeta.

Globalno zapošljavamo 2.000 ljudi koji čine veliku Dechra obitelj u kojoj njegujemo kulturu koja podržava naše vrijednosti: (D)edication - posvećenost, (E)njoyment - uživanje, (C)ourage - hrabrost, (H)onesty - poštenje, (R)elationships - odnosi i (A)mbition - ambicija.  Naše vrijednosti opisuju naš način poslovanja od proizvodnje do marketinga.

Prilika

The successful Regulatory Affairs Administrator is responsible for administering the RA inbox, invoice coding, licenses distribution and archiving, ordering standard substances and samples for regulatory purposes, handling of legalization procedures, initiation of artwork creation process in the system,

The RA Administrator would also updating and maintaining regulatory activities in SAMI (Regulatory Information Management System), creating electronic submission based on available dossiers and for supporting registration procedures.

Odgovornost

Izazov

Što će biti vaš posao? U sklopu ovog radnog mjesta obavljat ćete širok raspon raznovrsnih zadataka te biti odgovorni za:

  • initiate artwork creation process in TWONA and perform RA approval after finalisation.
  •  Assist RA colleagues with overview lists, cost estimates.
  • Administer Regulatory email inbox and archive.
  • Update and maintain SAMI with the support from RA colleagues.
  • Ensure received invoices for RA are coded, approved and sent back to finance for payment in due course. Archive and keep an overview of paid invoices.
  • Compiling electronic submission for new submissions, renewals and variations based on prepared dossiers for EU territories.
  • Following approval of a submission ensure Marketing Authorisation is checked, that all documentation is archived according to agreed procedure and relevant documents/databases are updated. Finally ensure distribution of Marketing Authorisation information to all relevant colleagues.
  • Support RA colleagues with requesting various needed certificates and samples.

Idealan kandidat

Od vas očekujemo

U Dechri se ponosimo našim različitostima i prihvaćamo prijave svih kandidata koji udovoljavaju uvjetima za zapošljavanje. Poželjne karakteristike kandidata za ovu poziciju su

  • Ability to demonstrate a methodical, organised and flexible approach to work.
  • High level of attention to detail and ability to follow detailed procedures and processes. Effective listening, verbal and written communication skills.
  • Excellent interpersonal skills, with the ability to communicate effectively with all levels of a business, establishing and maintaining effective working relationships.
  • Ability to plan, organise and prioritise workload to meet deadlines. Professional approach. Ability to maintain a high level of confidentiality and discretion at all times.
  • 2 years or working experience. Fluent in spoken and written English. Computer literate with a working knowledge of Microsoft Office (including Word, Excel, and Outlook).

O društvu

O vašoj prijavi

Sve pristigle prijave pregledava naš interni tim privlačenja talenata. Kontaktirat ćemo vas ukoliko vaše iskustvo i vještine odgovaraju onome što tražimo.   Ako vam se ne javimo unutar sljedećih 28 dana, molimo ne budite obeshrabreni – vaš životopis možemo zadržati u bazi za slučaj da se pojavi odgovarajuća slobodna pozicija. Ujedno vas pozivamo da i dalje pratite našu stranicu karijera. Za dodatna pitanja, slobodno nas kontaktirajte na  posao@dechra.com.

Dechra Pharmaceuticals PLC

Prijavi se

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