LOM (Labeling Ops) – International Associate (12 Months Contract)
Kinh nghiệm: Từ 2 năm kinh nghiệm làm việc liên quan đến regulatory hoặc labeling
Yêu cầu bằng cấp: Đại học
Số lượng cần tuyển: 1
Ngành nghề: Đăng ký thuốc
Địa điểm làm việc: Hà Nội
Chức vụ: Nhân Viên
Hình thức làm việc: Mọi hình thức
Yêu cầu giới tính: Không phân biệt
Yêu cầu
Here Is What You Need (Minimum Requirements)
A BA/BS degree with 2-3+ years of experience
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
Basic understanding of regulatory requirements for labeling
Strong organizational skills
Excellent written and verbal communication skills
Ability to work independently and as part of a team
Attention to detail and accuracy
Ability to manage multiple tasks simultaneously
Basic project management skills
Bonus Points If You Have (Preferred Requirements):
Experience in the pharmaceutical or biotechnology industry
Familiarity with labeling software and databases
Knowledge of global labeling regulations
Experience with electronic document management systems
Strong interpersonal skills
Strong analytical skills
Ability to interpret and apply regulatory guidelines
Effective problem-solving skills
Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
Work Location Assignment: Hybrid
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Important Notice for Applicants
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Quyền lợi
Theo quy định của nhà nước và chính sách công ty
Chi tiết
Use Your Power for Purpose
As an Associate in International Labeling Operations at Pfizer, you will play a crucial role directly contributing to the improvement of patients' lives. Your work will ensure that our products are accurately labeled, meeting regulatory requirements and providing essential information to healthcare professionals and patients. This role offers a unique opportunity to make a tangible impact on global health while working with a team of dedicated professionals.
What You Will Achieve
In this role, you will:
Support preparation of labeling documents to ensure regulatory compliance.
Coordinate with cross-functional teams to gather necessary labeling information.
Support the maintenance of accurate records of labeling changes and approvals.
Support the development and implementation of labeling strategies.
Facilitate timely submission of labeling documents to regulatory authorities.
Contribute to project tasks and milestones, organizing work to meet deadlines.
Learn and apply basic team effectiveness skills within the immediate work team.
Make decisions within limited options to resolve basic problems under supervision.
Work in a structured environment using established procedures and seek guidance from colleagues.
Have work regularly reviewed for technical judgment, completeness, and accuracy, relying on supervisor's judgment.

