• Studying scientific and legal documents to check they meet legal requirements.
  • Gathering, evaluating, organizing, managing and collating information in a variety of formats.
  • Submitting information and responding to queries from bodies such as the Medicines and Healthcare products Regulatory Agency (MHRA).
  • Maintaining familiarity with company product ranges.
  • Planning, undertaking, and overseeing product trials and regulatory inspections.
  • Keeping up to date with changes in regulatory legislation and guidelines.
  • Offering advice about regulations, company policies, practices and systems.
  • Obtaining marketing permission.
  • Outlining requirements for labeling, storage, and packaging, and approving information leaflets and labels.
  • Liaising and negotiating with regulatory authorities.

Job Details

Functional Area:
Total Positions:
1 Post
Job Shift:
First Shift (Day)
Job Type:
Job Location:
Gender:
Male
Minimum Education:
Bachelors
Degree Title:
Biotechology, Biochemistry, medical devices
Career Level:
Entry Level
Experience:
Less than 1 Year - 2 Years
Apply Before:
Jun 22, 2024
Posting Date:
May 21, 2024

HealthBee Projects

Pharmaceuticals / Clinical Research · 301-600 employees - Islamabad, Rawalpindi

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