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RA/PV Specialist

  South of Malta

Our client who specialises in the pharmaceutical industry is looking for a RA/PV Specialist. Your roles and responsibilities will include: 

  • Preparing, submitting, tracking, and archiving technical documentation, amendments, reports, and correspondence related to EU filing submissions. 
  • Ensuring timely submissions to competent authorities and maintaining organized records
  • Prepare and submit regulatory documents for EU filings
  • Track the status of submissions and maintain an organized archive of technical documents and correspondence
  • Collaborate with regulatory teams to ensure timely and accurate submissions to EU authorities

Requirements

  • Strong written and verbal communication skills, with the ability to convey complex technical and scientific information clearly
  • Team-oriented with excellent collaboration abilities
  • Science Degree or similar

Education and Experience

  • 3 to 5 years of proven experience in Regulatory Affairs or Pharmacovigilance

Benefits

  • Health Insurance

Job Reference: CM443

  • Category
    Quality Assurance
  • Job type
    Full Time
  • Employment level
    Intermediate (1-3 years)
  • Work Location
    On Premises
  • Employer industry
    Pharmaceuticals
  • Languages
    English, Maltese
  • Job Reference
    CM443
  • Closing Date
    31/10/2024
  • Date Published
    23/10/2024
  • Status
    Shortlisting

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