Kenvueは現在、以下求人を募集しております。
Executive - External Manufacturer Quality (Food)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:
General Q&C Manager場所:
Asia Pacific, India, Maharashtra, Greater Mumbai勤務地:
フルオンサイトあなたがすること
Kenvue is currently recruiting for:
Executive - External Manufacturer Quality (Food)
This position will be based out of Mumbai (India)
Who We Are
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. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of 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.
Position Summary
The role is responsible for implementing, maintaining, and continuously improving the Quality System (QS) in accordance with local and global regulatory (GMP, D&C Act, ICH, FSSAI, CODEX) and Kenvue internal QS requirements. This role ensures compliance, data integrity, and operational excellence across all quality system elements in a commercial or manufacturing environment.
Key Responsibilities
1. Quality Management System (QMS) deployment
Maintain and enhance the QMS aligned with GMP, FSSAI, and company standards.
Own or support QMS modules such as Change Control, Deviation Management, CAPA, Document Control, Complaint Handling, and Supplier Quality.
Monitor QMS KPIs and generate periodic quality dashboards for periodic Management Reviews.
2. Documentation & Change Control
Review, approve, and control GMP documentation (SOPs, specifications, batch records).
Evaluate and coordinate changes through the Change Control system ensuring proper risk assessment.
3. Deviation, Investigation & CAPA Management
Lead or support investigations for deviations, OOS/OOT, and incidents.
Ensure timely closure of CAPAs and effectiveness checks.
Apply structured problem-solving tools (Root Cause Analysis, 5-Why, Fishbone).
4. Internal & External Audits
Plan and execute internal audits as per the audit schedule.
Support regulatory inspections and customer audits.
Prepare and track audit action plan and ensure effective closure.
5. Training & Compliance
Maintain training matrices and ensure role-based GMP training compliance.
Conduct training on quality systems, data integrity, and regulatory updates.
6. Data Integrity & System Compliance
Ensure ALCOA+ principles are implemented across all quality processes.
Participate in validation and qualification of GxP systems.
7. Supplier Qualification
Support supplier qualification, audits, and ongoing performance monitoring.
Manage quality agreements.
8. Continuous Improvement
Identify opportunities to streamline QMS processes.
Implement Lean, Six Sigma, and digital quality improvements.
Qualifications & Experience
Bachelor’s/Master’s in Pharmacy, Chemistry, Biotechnology, Food technology or related field.
5–7 years of experience in Quality Assurance / Quality Systems (depending on seniority) preferably in food .
Strong knowledge of GMP regulations: ICH Q10, EU GMP, WHO, 21 CFR parts 210/211.
Experience with electronic QMS systems (TrackWise, EtQ, Veeva) preferred.
Good analytical, documentation, and communication skills.
Key Competencies
Strong understanding of pharmaceutical manufacturing and control systems.
Excellent problem-solving and root‑cause analysis capabilities.
Ability to work cross‑functionally with Operations, Technical Operations, Engineering, and R&D.
High attention to detail, integrity, and compliance mindset.
Ability to manage multiple priorities in a dynamic environment.
What’s In It For You
- Competitive Benefit Package
- Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & 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 identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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