Kenvueは現在、以下求人を募集しております。
Pharmacovigilance Specialist [remote 12 months fixed-term]私たちがしていること
私たちKenvueは、日々のケアが持つ驚くべき力を信じています。100年以上の伝統と科学に根ざし、Neutrogena®, Aveeno®, Tylenol®, Listerine®, Johnson’s® and BAND-AID®など、皆様が既にご存じでご愛用いただいているアイコニックなブランドを提供しています。科学は私たちの情熱であり、ケアは私たちの才能です。
Who We Are
私たちのグローバルチームは、インサイトとイノベーションに情熱を注ぎ、最高の製品をお客様にお届けすることに全力を注ぐ、多様で優秀な22,000人以上の社員で構成されています。専門知識と共感力を備えたKenvuerであることは、毎日何百万人もの人々の生活に影響を与える力を持つことを意味します。私たちは、人を第一に考え、全身全霊をもってケアし、サイエンスで信頼を獲得し、勇気をもって解決します。私たちとあなた自身の未来を、共に切り開いていきましょう。
Role reports to:
Mgr Loc Pharmacovigilance Contract Lead場所:
Latin America, Brazil, Sao Paulo, Sao Paulo勤務地:
完全リモートあなたがすること
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.
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