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Sr. Manager Global Regulatory Compliance

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Sr. Manager Global Regulatory Compliance

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 :

DIRECTOR, REGULATORY COMPLIANCE (APAC)

Lieu :

Asia Pacific, Singapore, Singapore, Singapore

Lieu de travail :

Hybride

Ce que tu vas faire

The Senior Manager, Global Regulatory Compliance (GRC), is responsible for maintaining sustainable compliance programs that are aligned with Kenvue Regulatory Compliance processes, as well as segment and franchise requirements. This role will provide cGMP compliance insight for key operational activities regulated by local Health authorities, and other relevant regulatory bodies. This role will work closely with site quality, compliance, operations, and technical operations leadership to cultivate GMP awareness, issue identification, risk mitigation, inspection readiness, and BOH management. This role will have responsibility for maintaining relationships through interdependent partnering and forming alliances with cross functional business partners to drive compliant completion of key goals and objectives. This position will primarily support the Kenvue businesses within China, and other APAC markets as appropriate

Key Responsibilities

  • Lead regulatory compliance and quality risk management activities across assigned sites, proactively identifying, assessing, and escalating compliance risks to leadership.

  • Monitor compliance performance through data analysis, quality records reviews, audits, inspections, investigations, CAPAs, complaints, and regulatory communications.

  • Drive timely resolution of compliance issues by partnering with site teams on corrective and preventive actions (CAPAs), risk mitigation plans, and continuous improvement initiatives.

  • Provide expert guidance on cGMP requirements, regulatory expectations, quality systems, and critical quality or regulatory compliance matters.

  • Support Health Authority inspections and audits by preparing sites, facilitating inspection readiness, managing responses, and overseeing post-inspection commitments.

  • Collaborate with site leaders, process owners, and cross-functional stakeholders to ensure compliance considerations are embedded in product lifecycle management, supply chain projects, and quality system changes.

  • Maintain alignment of site policies and standards with corporate requirements while providing insight into new and emerging regulatory expectations across the APAC region.

  • Participate in governance forums, crisis management, and enterprise compliance programs to strengthen risk management, drive strategic consistency, and promote a culture of quality and compliance.

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    What We Are Looking For

    Required Qualifications

    • Bachelor’s degree required; advanced degree preferred, ideally in Science, Engineering, or a related technical discipline.

    • Minimum 8 years of experience in Quality, Compliance, Manufacturing, or Operations within the pharmaceutical, medical device, or cosmetic industries; China experience strongly preferred.

    • Strong knowledge of APAC and Chinese GxP regulations, GMP requirements, and regulated manufacturing environments.

    • Experience supporting regulatory inspections, responding to Health Authority observations, and managing compliance within quality systems.

    • Proven ability to analyze data, manage complex projects, and operate effectively in global and multicultural environments.

    Who Are You?

    • A strategic and independent problem solver who can assess risks, make sound decisions, and drive solutions in complex business environments.

    • A strong leader and collaborator with the ability to influence, negotiate, and build trusted relationships across cross-functional teams.

    • An effective communicator who can translate complex technical and regulatory information into clear business recommendations; fluent in both English and Chinese.

    • A change agent who can navigate resistance, foster alignment, and lead stakeholders through regulatory and quality initiatives.

    • A results-driven professional with strong organizational skills and proficiency in MS Office tools, analytics, and presentation software.

    What’s In It For You

    • Competitive Benefit Package

    • Paid Company Holidays, Paid Vacation, Volunteer Time & 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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