。该工作已被公司管理人员暂停申请，不再接受简历投递
发布 May 21, 2024 418 查看
- 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.
HealthBee Projects
· 301-600 员工 - 伊斯兰堡, 拉瓦尔品
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