Kenvue 目前正在招聘 a：
我们做什么
在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。
我们是谁
我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.
Role reports to：
QPPV HEAD OF SAFETY SCIENCE AND POLICY位置：
Asia Pacific, Philippines, National Capital, Paranaque工作地点：
混合你会做什么
The Junior Global Risk Assessment Safety Physician (JGRASP) provides medical assessment of the product information pertinent to safety risk assessment and characterization of the emerging and known product safety profiles for assigned Kenvue portfolio products. The JGRASP also ensures communication of potential and known risks, when appropriate, to direct management, regional medical management, Qualified Person for Pharmacovigilance (QPPV), and personnel in all other relevant functional areas. The JGRASP is responsible for providing medical assessment of individual and aggregate safety data, support safety concerns and safety signals assessment, development of ad hoc safety reports and PSURs/PBRERs. He/She may be assigned development and/or ownership of processes, as needed, and shall ensure that performed activities fulfill the relevant regulatory requirements and all applicable Kenvue processes.
Key Responsibilities
Safety data assessment and medical insights on safety deliverables for assigned products, including but not limited to:
- Review safety data available from external and internal sources including spontaneous adverse event reports, safety data from non-spontaneous (solicited sources), results of signal detection
- Evaluation and communication of safety-related concerns (including ESI/SSI)
- Contribution to the development of signal detection strategy
- Contribution to the development of ad hoc reports
- PSUR/PBRER reviews
- Advice on risk mitigation actions
- Contribution to safety plans for new products and indications
- Incorporates new safety data into clinical practices and initiates core data sheet and label changes.
- Gathering safety data for responding to queries from Regulatory Authorities, commercial partners and internal stakeholders on safety concerns and risk management including development of appropriate documentation
- Guides analysis of database and literature searches, making conclusions about the safety signal or efficacy (or lack thereof).
- Documents results of the data review and the conclusions, actions, and advice given.
- Leads special projects related to drug and product safety.
What We Are Looking For
Key Qualifications
- A Licensed Physician
- Relative experience is preferred but not required
- Demonstrated ability to critically evaluate and analyze safety data from multiple sources (post-market reports, literature, etc.), and communicate findings to inform stakeholders
- Demonstrated ability to understand the clinical application/use of the technology/medication/product and assess the potential for a safety risk and need for risk minimization
- Demonstrated ability to carry out structured problem-solving and decision-making skills
- Demonstrated ability to communicate effectively complex topics with cross functional stakeholders
- Highly passionate in making a positive impact consumers’ lives
What’s In It For You
- Competitive Benefit Package
- Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!
- Learning & Development Opportunities
- Employee Resource Groups
- Flexible Work Arrangements
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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