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：
Mgr Loc Pharmacovigilance Contract Lead位置：
Latin America, Brazil, Sao Paulo, Sao Paulo工作地点：
完全远程你会做什么
The Pharmacovigilance Specialist will support the Local Pharmacovigilance Organization (PV) in several PV processes and compliance tasks related to the vigilance of the Kenvue product portfolio, under the umbrella of the Local Safety Officers (LSOs).
This position will be based out of São Paulo and the selected candidate will be required to be in the office at least 1x or 2x per month for collaboration with the team.
Please submit your resumé in English.
Responsibilities:
• Support the LSOs on applicable operational tasks and ensure overall inspection readiness across the Local Pharmacovigilance Organization, collaborating closely with team members from all regions to ensure a consistent global approach to Safety.
• PV Contract Management:
o Manage and maintain oversight local PV agreements across all regions.
o Ensure local agreements are reviewed to assess if a Pharmacovigilance (PV) agreement is recommended.
o Review the draft PV Agreement to ensure its accuracy and support negotiation with External Partners and execution in partnership with LSOs.
o Ensure accuracy of PSMF Annex B Service and Technical Agreements listing.
o Contribute to process improvement initiatives related to local PV agreement management.
• Procedural Document:
o Develop, update, and implement LPV procedures to ensure compliance with Kenvue global procedures and local requirements.
o Ensure current knowledge of all relevant company procedures and training.
What we are looking for
Desired Qualifications
o Qualification in Medical/ Health Sciences and/or proven equivalent experience in pharmacovigilance and safety issue management
o Experience in Pharmacovigilance
o Fluent communication skills in English, any additional language is a plus.
o Ability to connect in a global organization.
Desired Qualifications
o Proven ability to organize workflow activities.
o Awareness of and familiarity with industry principles of product vigilance, drug development, and pharmacology.
o Knowledge of global, regional, and local procedural documents as applicable.
o Computer literate with knowledge of relevant IT safety systems.
o Good verbal and written communication skills.
o Ability to establish and maintain open relationships within the organization.
What’s in it for you
• Competitive Total Rewards Package*
• Paid Company Holidays, Paid Vacation, Volunteer Time & More!
• Learning & Development Opportunities
• Employee Resource Groups
• This list could vary based on location/region
*Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.
如果您是残障人士，请查看我们的 残障人士援助页面了解如何申请便利
