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Posted May 21, 2024 418 views
- 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
Industry:
Functional Area:
Total Positions:
1 Post
Job Shift:
First Shift (Day)
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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