Kenvueは現在、以下求人を募集しております。
Scientist, R & D Materials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:
Principal Scientist RMC Analytical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:
Scientist – R&D Materials Team
This position reports to Manager, R&D Materials and is based at 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® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse and brilliant people, passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact the 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.
Role reports to: Manager, R&D Materials team
Location: Mulund, Mumbai, India
Travel %: 5 %
What you will do
- The Scientist, R&D Materials team is responsible for supporting various RM qualification projects globally for specification management and change impact assessment to ensure the compliance to the current regulatory and industry standards, and internal requirements for Cosmetic & OTC portfolio.
Key Responsibilities
- To provide technical assessment of Raw materials used at Internal and External Manufacturing sites to ensure alignment with current compendia, industry standards, product registrations, and internal procedures.
- To write and/or coordinate specifications and/or change control by adhering to the internal procedures, GxP requirements and right first-time principle
- Approve specifications and change controls and provide timely input to the Specification/Change control authors on the area of improvement.
- To collaborate with Global sites and the Specification team business partners and stakeholders (Internal/External Manufacturing Sites, Regulatory, Quality etc) to drive best practices for RM specifications aligned with company goals and objectives.
- This person will be responsible for understanding the impact of global Pharmacopoeia monographs on our products and owing changes to the impacted sites to ensure compliance, before effective dates.
- Maintain a results-oriented focus, consistently delivering on business objectives.
- Collaborate with the external partners for outsourcing activities related to RM specifications
- Make fact-based decisions regarding analyzing and interpreting data, drawing conclusions, and arriving at timely technical decisions
- Demonstrate clear engagement for action on priorities and get the projects targets demonstrating a great sense of urgency.
What we are looking for
Required Qualifications
- Minimum of a bachelor’s/ Masters degree in Chemistry (Analytical / Organic) /Pharmaceutical Chemistry /Life Sciences with 3-5 years of experience in Pharma or FMCG sector
Desired Qualifications /Skills
- Experience in a GxP environment is required
- In depth understanding & hands on experience of Analytical testing is required
- Experience with use of Microsoft's suite of products (Excel, Word, PowerPoint) is required
- Experience with quality compliance systems is preferred
- Experience with Consumer products (OTC and Cosmetic) is preferred.
- Effective communication skills, as this role requires consistent, frequent collaborations with global sites, project teams, and outsourced technical writers, via virtual meetings and email correspondences
- Strategic and operational skills to prioritize and execute projects based on business and compliance needs
- High level of learning agility and problem-solving skills
What’s in it for you
- Annual base salary for new hires in this position takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.
- 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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