International Regulatory Affairs Senior Specialist

Acino Pharma

Employer Active

Posted 14 hrs ago

Experience

2 - 7 Years

Job Location

Egypt - Egypt

Education

Bachelor of Pharmacy(Pharmacy)

Nationality

Any Nationality

Gender

Not Mentioned

Vacancy

1 Vacancy

Job Description

Roles & Responsibilities

Completes low and medium regulatory complex assignments

  • Plans, prepares, compiles and submits high-quality regulatory applications in compliance with applicable requirements for each region/country
  • Prepares electronic submission files in the document management tool docuBridge and submits regulatory dossiers via CESP (EU) and the portal of Swissmedic (CH)
  • Prepares electronic submission files in the electronic document management system and dispatches them to Regional Regulatory Affairs Teams or third parties
  • Tracks the status of applications under regulatory review and provides updates to the regulatory team or other internal/external stakeholders
  • Revises and approves artwork of product packaging material in internal system, according to applicable guidelines
  • Schedules meetings with internal stakeholders, third parties or regulators and develops and organizes material for these meetings and participates at these meetings
  • Maintains ARCERA s internal regulatory information management system, and other databases
  • Uploads product information texts to health authority webportals
  • Calculates and tracks sunset clause dates and notification of supply interruption in EU markets and Switzerland
  • Ensures regulatory compliance
  • Adheres to standard operating procedures and other applicable legislation
  • Communicates information on regulatory requirements to other departments
  • Attends to internal trainings in due time
  • Provides regulatory support to project teams, stakeholders and customers, as required.
  • Forwards all received Product Quality Complaints, Adverse Events, and Medical Information Requests to the relevant person in Quality Assurance, Pharmacovigilance, and Medical Affairs
  • Performs other tasks under the direction of the Manager within the agreed type of work


Key Skills:

  • Acts in accordance with ARCERA principles and values
  • Good communication skills, both verbal and written, with a passion for accuracy and attention to detail.
  • Good interpersonal skills ability to effectively interact with a diverse group of people from different functions, of different nationalities and at different levels within the company or external business partners.
  • Good project management skills.
  • Willingly accepts challenging assignments and new career opportunities that stretch and build capabilities.

Desired Candidate Profile

Qualifications & Experience:

  • Two or more years of regulatory affairs experience in relevant discipline (experience in a similar position is of advantage)
  • Profound knowledge of regulatory requirements, process, procedures & pathways
  • Profound knowledge of regulatory life cycle management of pharmaceutical products
  • Experience in working in project teams
  • The minimum educational requirement is a bachelor s degree in pharmacy, chemistry, biology, or another life science.
  • Business English at least at intermediate level

Company Industry

Department / Functional Area

Keywords

  • International Regulatory Affairs Senior Specialist

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