Assistant Manager Supplier Quality

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在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。

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我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.

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What we do

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

 Who we are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights and innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours. For more information, click here.             

Role reports to: Supplier Quality Manager

Location: Mumbai India

Travel %: (10-20%)

What you will do

Assistant Manager Supplier Quality is responsible for supporting supplier quality operations across multiple categories by maintaining quality systems, coordinating change control activities, supporting audits, and driving corrective and preventive actions. This role acts as a generalist within the Supplier Quality organization, partnering cross-functionally to ensure compliance, inspection readiness, and continuous improvement across the supply base.

Key Responsibilities

• Conduct supplier qualification, surveillance, and for-cause audits to assess compliance with Kenvue quality standards and applicable regulatory requirements.
• Evaluate supplier adherence to relevant regulations and GMP requirements, including CDSCO, Local FDA, and Schedule M.
• Manage supplier audit programs, ensuring timely execution, reporting, and closure of audit CAPAs.
• Review and verify the adequacy and effectiveness of supplier-provided evidence for closure of audit observations.
• Support supplier-related change controls and assess quality impact to ensure compliance and continuity of supply.
• Partner with suppliers to investigate and resolve quality system issues, non-conformances, and compliance gaps.
• Perform supplier risk assessments and drive implementation and follow-up of mitigation plans.
• Lead closure of supplier quality action plans, escalations, remediation activities, and supplier exit strategies, as required.
• Support the Supplier Reliability Program by improving supplier quality, delivery performance, compliance, and continuous improvement.
• Collaborate cross-functionally with suppliers, Procurement, Manufacturing, Regulatory Affairs, and Quality teams to maintain robust supplier quality management systems.

What we are looking for

Required Qualifications

• Minimum 5-8 years of experience in Quality Assurance/Quality Systems, including supplier qualification, supplier audits, and external manufacturer oversight within the pharmaceutical, consumer healthcare, or FMCG industry.
• Strong knowledge of applicable regulatory requirements and quality standards, including Drugs & Cosmetics Act, CDSCO guidelines, ICH guidelines, 21 CFR Parts 210 & 211, FSSAI, BRC, and current GMP requirements.
• Proficient in the use of digital tools and IT applications for preparing quality documentation, business correspondence, presentations, training materials, and management reports.
• Effective communication, stakeholder management, and CAPA management skills, with the ability to drive robust Quality Management System (QMS) compliance.
• Sound understanding of Change Control, Deviation Management, Risk Assessment, Internal Audits, CAPA, and cGMP requirements.
• Hands-on experience in Quality Assurance (QA) or Quality Control (QC) within API, pharmaceutical formulation, chemical, excipient, packaging material
• Demonstrated ability to collaborate effectively with suppliers and cross-functional teams to drive compliance, quality improvement, and inspection readiness.

Desired Qualifications

• ISO 9001:2015 Lead Auditor/Internal Auditor certification or equivalent quality management certification is preferred and will be considered an added advantage.
• Demonstrated ability to lead complex supplier quality initiatives and cross-functional projects involving global suppliers and multiple stakeholders.
• Strong analytical and problem-solving skills, with the ability to translate quality data and trends into effective risk mitigation and continuous improvement actions.
• Proficiency in digital Quality Management Systems (eQMS), data analytics, and reporting tools, including Veeva Vault, ETQ NxG, Power BI, and Microsoft Office applications; commitment to continuous learning and adoption of emerging quality technologies.
• Excellent communication, influencing, and stakeholder management skills, with the ability to build productive partnerships across global suppliers, manufacturing sites, Procurement, and Quality organizations.

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