Regulatory Affairs Manager (f/m/d)

Regulatory Affairs Manager (f/m/d)

Randstad Deutschland GmbH & Co. KG

Lokalizacja

Hexjobs Insights

Stanowisko: specjalista ds. regulacyjnych w przemyśle farmaceutycznym. Obowiązki: wsparcie w tworzeniu dokumentacji produktów. Wymagania: wykształcenie wyższe w naukach przyrodniczych, doświadczenie, dobra znajomość języka angielskiego.

Słowa kluczowe

specjalista ds. regulacyjnych
dokumentacja techniczna
zgody federalne
zarządzanie dokumentami
przemysł farmaceutyczny
Microsoft Office
znajomość języków

Benefity

  • Bożonarodzeniowe i urlopowe premie
  • Do 30 dni urlopu rocznie
  • Składka na program emerytalny po okresie próbnym
  • Szeroki wachlarz dodatkowych benefitów dla pracowników

Firmenbeschreibung

Time for change – time for a new job! You are a regulatory affairs specialist and looking for a new professional challenge? Then stop searching! We offer the job you are looking for: Our subsidiary Randstad professional solutions offers a secure job, fair compensation and exciting new tasks at an attractive pharmaceutical company in Ludwigshafen. Apply online now! We welcome applications from all suitably qualified persons regardless of any disabilities.

Ihre Aufgaben

  • Provide support to complete product dossiers, technical files and responses to information requests
  • Coordinate and complete documents required by federal agencies, incl. maintaining complex files and electronic document management systems
  • Work with project teams to obtain approval for company products
  • Serve as the primary point of contact for federal governmental agencies, embassies and consulates in Germany and function as center of excellence for requests
  • Gather documents from all EU facilities required for product registration in applicable countries/regions
  • Coordinate document requests for products approved via the Centralized Procedure (CP) but are manufactured in Germany
  • Work directly with third party manufacturing companies to obtain documents

Unsere Anforderungen

  • Bachelor's degree in life science, clinical research studies or engineering, ideally with previous regulatory experience
  • Several years of experience in a regulated business environment (e.g. legal office, regulated industry)
  • Experience working with Microsoft Office suite, most notably with Excel, Word, Outlook, Teams, and Microsoft SharePoint tools
  • Working knowledge of database management
  • Knowledge on current policies and practices issued by local German federal agencies
  • Awareness on regulatory policies/procedures to learn and better understand how the landscape of regulations develops
  • Good proficiency in the English language
  • Strong negotiation and communication skills as well as ability to organize data and identify issues or gaps in documentation

Das dürfen Sie erwarten

  • Above-average salary
  • Extensive social benefits, incl. Christmas and holiday bonuses
  • Up to 30 days vacation per year
  • Company pension scheme contribution after the end of the probationary period
  • A wide range of employee benefits/perks

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Wyświetlenia: 2
Opublikowana2 dni temu
Wygasaza 28 dni

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