Kenvueは現在、以下求人を募集しております。
Associate Scientist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
JOB TITLE : ASSOCIATE SCIENTIST, ANALYTICAL CHEMISTRY
Company : Kenvue, JNTL Consumer Health India Pvt Limited
Location : Mulund, City : Mumbai, Country : India
Department : R&D Analytical Operations
Function : Analytical Chemistry
ABOUT THE ROLE
The objective of this position is to deliver analytical services to various Kenvue Consumer Health Global R&D sites for multiple product categories under various franchises such as Self Care (OTC drugs), Skin Health and Essential Health (Baby care, Oral Care, etc.) etc.
The Associate Scientist position will be a part of the team that is responsible for analytical deliverables of new product development projects, support changes to commercial products and specific research-based activities assigned as a part of Global operations. The key role is to deliver the analytical testing and related documentation activities with a compliance focus under the supervision of the team leader.
JOB RESPONSIBILITIES
- ANALYTICAL DETERMINATIONS AND TECHNICAL ASSESSMENTS :
- Ensure qualification on assigned analytical technologies and instrumentation for testing capabilities.
- Conduct testing on assigned analytical technologies such as HPLC/ UPLC, GC, IC, AAS etc.
- Execute the assigned stability testing for shelf-life assessment of stability studies.
- Responsible for method validation activities including technical documentation under the guidance of the team leader.
- Participate in method transfer process regarding testing activities under supervision.
- SUPPORT TO EQUIPMENT MANAGEMENT PROGRAM :
- Responsible for assigned calibration activities for lab instrumentation and technology.
- TECHNICAL DOCUMENTATION :
- Partner with key responsible for providing data in technical documents e.g. stability reports, method transfer, method validation protocol and reports, etc.
- LAB PROCESS/QUALITY SYSTEMS MANAGEMENT:
- Diligently follow and execute (as required) assigned responsibilities in compliance with critical laboratory processes and quality systems.
- Focus on basic lab processes and requirements during work and escalate wherever required.
- ENGAGEMENT ON SITE INITIATIVES:
- Participate and collaborate with site cross functional teams for assigned deliverables when nominated on such forums.
TECHNICAL COMPETENCIES
- Basic technical expertise related to chemistry, analytical techniques, stability study assessment
- Diligent execution of analytical projects with a right first-time approach.
- Basic knowledge of current GMP, quality systems, site specific SOPs, regional/Global technical requirements
- Overall awareness related to instrumentation principles and working, good documentation practices, data integrity aspects, etc.
- Ability to work with digital tools and software applications
LEADERSHIP COMPETENCIES
- Ability to grasp technical/compliance requirements and execute assigned work to meet the key performance indicators
- Good oral and written communication skills
- Challenges the status quo and brings innovative ideas and suggestions
- Displays technical curiosity and self-initiative to deliver beyond usual activities
- Good interpersonal skills to partner within team
EDUCATION/WORK EXPERIENCE REQUIREMENTS:
- Education: Minimum MSc, B Pharm, M. Pharm, Ph.D. or equivalent science stream
- Other Skills: MS office advanced
- Work experience : Minimum 1 to 3 years in Analytical development, Quality Control or related functions in healthcare/pharma/FMCG sector with exposure to GMP, 21 CFR Compliance and Quality environment preferred.
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