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Global Risk Assessment Safety Physician

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Kenvue recrute actuellement pour un :

Global Risk Assessment Safety Physician

Ce que nous faisons

Chez Kenvue, nous réalisons le pouvoir extraordinaire des soins quotidiens. S'appuyant sur plus d'un siècle d'héritage et enraciné dans la science, nous sommes la maison de marques emblématiques - dont NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® et BAND-AID® que vous connaissez et aimez déjà. La science est notre passion ; Le soin est notre talent.

Qui nous sommes

Notre équipe mondiale est composée de ~ 22 000 personnes brillantes avec une culture d'entreprise où chaque voix compte et chaque contribution est appréciée. Nous sommes passionnés par les idées, l'innovation et l'engagement à fournir les meilleurs produits à nos clients. Avec de l'expertise et de l'empathie, être un Kenvuer signifie avoir le pouvoir d'avoir un impact sur des millions de personnes chaque jour. Nous donnons la priorité aux personnes, nous nous soucions farouchement, nous gagnons la confiance grâce à la science et nous résolvons les problèmes avec courage - et nous vous offrons de brillantes opportunités ! Joignez-vous à nous pour façonner notre avenir et le vôtre. Pour plus d'informations, cliquez sur ici.

Role relève à :

QPPV HEAD OF SAFETY SCIENCE AND POLICY

Lieu :

Asia Pacific, Philippines, National Capital, Paranaque

Lieu de travail :

Hybride

Ce que tu vas faire

The Global Risk Assessment Safety Physician (GRASP) is a medical safety expert who provides medical oversight of the product safety risk assessment and characterization of the emerging and known product safety profiles for assigned Kenvue portfolio throughout the product lifecycle. The GRASP 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. He/She is responsible for the development strategy of safety concerns assessment, ad hoc safety reports, safety signal management, PSURs/PBRERs, risk management, internal and external due diligence activities, provides recommendation for risk minimization if deemed and chairs Safety Management Team (SMT) meetings.  He/She leads, under direction of the Head of Global Safety Risk Management, the strategy of responding to queries from Regulatory Authorities, commercial partners and internal stakeholders on safety concerns and risk management, and may be assigned ownership of processes or vendor oversight, as needed, and shall ensure that performed activities fulfill the relevant regulatory requirements and all applicable Kenvue processes.

Key Responsibilities

- Medical insights on safety deliverables for their assigned portfolio, 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)
  • Chairing periodic Benefit-Risk Review by the SMT
  • Development of signal detection strategy
  • Development of ad hoc reports
  • PSUR/PBRER strategy and reviews
  • Advice on risk mitigation actions including providing direction at Labeling Working Groups (LWGs) and other relevant portfolio forum/Committees
  • Providing support for due diligence activities
  • Development of safety plans for new products and indications
  • Leading strategy of responding to queries from Regulatory Authorities, commercial partners and internal stakeholders on safety concerns and risk management including development of appropriate documentation
  • Approval of safety-related content for press releases and other public and professional communications
  • Initiates escalation of safety signals/concerns to the Medical Safety Council (MSC) and senior management as appropriate

- Ensures strategic safety insights are applied to oversight of queries from the safety and medical teams on safety-related content and study protocols.

- Process development and ownership, potentially including vendor oversight

What we are looking for

Required Qualifications

  • Physician (MD) with at least 3 years clinical experience.
  • Five or more years industry experience in medical safety is preferred.
  • Ability to analyze, interpret and present complex data in a concise and understandable scientific manner, both orally and in written format, is essential.
  • Critical thinking and agility in the evaluation of safety topics and development of processes
  • Attention to detail, and diligence in record-keeping and records organization
  • Ability to manage high workload and critical issues
  • Computer-literate and proficient in MS Office applications
  • Team player who displays initiative, have strong communication and presentation skills
  • Strong collaborative and interpersonal skills
  • Results-oriented and able to independently create and deliver
  • Ability to thrive in a global, cross-functional environment.

What’s in it for you

  • A dynamic opportunity to work in one of Kenvue’s fastest growing and most high profile businesses, with visibility to both global and regional stakeholders.
  • Competitive Benefit Package
  • Flexible Work Arrangement, Volunteering Days, Health and Wellness Reimbursements and much more!
  • Learning & Development Opportunities
  • Employee Resource Groups 

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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