Θέσεις εργασίας στην Ελλάδα

Η αγγελία εργασίας έχει λήξει

27/05/2022

Regulatory Affairs Project Manager (1-year contract)

Διοίκηση Επιχειρήσεων - HR - Στελέχη

Πόλη ΑΘΗΝΑ ΒΟΡΕΙΑ ΠΡΟΑΣΤΙΑ | ΑΘΗΝΑ - ΑΤΤΙΚΗ
Απασχόληση Πλήρης απασχόληση

Περιγραφή

ManpowerGroup Greece, on behalf of its client, a multinational healthcare
company, is searching for a Regulatory Affairs Project Manager, who will be responsible for the management of all end-to-end regulatory activities within the scope of a challenging project for the local Medical Devices company.

Workplace Location: Northern Suburbs of Athens / Hybrid model
Working hours : 09:00-17:30

Main responsibilities:

  • Drives the communications with business partners to ensure optimal internal and external interaction within project scope and in alignment with business plans
  • Ensures compliance of project deliverables with EU & local legislation and applied Enterprise Quality Standards
  • Develops and execute a proper strategy for the project implementation
  • Oversights a local team of contractors: defines goals and objectives, provides on-the-job training, monitors work progress, assists on project deliverables, if needed
  • Ensures efficient management of end-to-end regulatory activities under the scope of this project in compliance with local legislation and in alignment with business objectives
  • Partners with Supply Chain and Franchise Regulatory teams to ensure supply continuity during the transitional period
  • Partners with relevant functions (commercial, tendering, finance) to define plan for a smooth project execution
  • Provides Regulatory insights to the global, regional and local teams on project related activities
  • Supports Tendering and Marketing Depts to ensure that Regulatory documentation impacted by the project, for all marketed products is updated and available for all necessary purposes
  • Shapes regulatory environment in relation to the scope of the project through communication with external stakeholders

Απαραίτητα Προσόντα

Candidate Profile:
  • At least 4 years of proven working experience in the field of Medical Device and/or Pharma Regulatory Affairs
  • Experience on Project Management is required
  • Experience in People leadership desired
  • Experience and knowledge of local MD legislation
  • Bachelor’s/ Master’s Degree in Life Sciences/related field will be an asset
  • Proficiency in Microsoft applications (Word, Excel, PowerPoint etc.)
  • Proficiency in the English Language
  • Strong collaboration and communication skills and ability to build partnerships internally and externally at a global network
  • Ability to work under strict timelines, combined with flexibility when emergency situations require this
  • Strong organizational skills, including the ability to prioritize workload

Παροχές

Remuneration Package:
  • Competitive gross monthly salary
  • Company laptop
  • Meal Vouchers
  • Excellent training and development opportunities within a multinational company