Scientist

2 weeks ago


Mumbai, Maharashtra, India Kenvue Full time
Scientist W Description

Kenvue is currently recruiting for:

Scientist

This position reports into Principal Scientist and is based at Greater Mumbai.

Who We Are

At , 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 up with 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, .

What You Will Do

The position is responsible for:

·Delivering 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 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.

Key Responsibilities

ANALYTICAL DETERMINATIONS AND TECHNICAL ASSESSMENTS:

·Ensure qualification on a wide range of analytical technologies and instrumentation for testing capabilities.

·Execute the assigned stability testing for shelf-life assessment of stability studies.

·Responsible for method development and subsequent method validation activities including technical documentation under the guidance of the team leader.

·Participate in method transfer process regarding testing activities.

·Work on specific research projects, if required.

SUPPORT TO EQUIPMENT MANAGEMENT PROGRAM:

·Responsible for assigned qualification and calibration activities for lab instrumentation and technology.

·Deliver the instrument owner role for basic lab equipment 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:

·Support process owners or subject matter experts for assigned responsibilities, critical laboratory processes and quality systems.

·Provide oversight for basic lab processes and escalate wherever required.

ENGAGEMENT ON REGIONAL/GLOBAL INITIATIVES:

·Participate and collaborate with regional and Global teams for assigned deliverables when nominated on such forums.

Qualifications

What We Are Looking For

Required Qualifications

·Education: Ph.D. (Pharmacy, Chemistry) from a reputable institute preferred. MSc, B Pharm, M. Pharm, or equivalent science stream.

·Other Skills: MS office advanced

·Work experience: Minimum 3 years and up to 6 years in Analytical development, Quality Control, or related functions in healthcare/pharma/FMCG sector with exposure to 21 CFR Guidelines, GMP and Quality environment must.

Desired Qualifications

·Effective planning and execution of analytical projects independently

·Ability to grasp technical/compliance requirements and execute assigned work to meet the key performance indicators.

·Excellent oral and written communication and articulation 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 across functions, sites, and regions.

·Sound technical expertise related to chemistry, analytical techniques, stability study assessment.

·Diligent execution of analytical projects with a right first-time approach.

·Adequate knowledge of current GMP, quality systems, site specific SOPs, regional/Global technical requirements

·Technical skills related to instrumentation principles and working, basic troubleshooting, good documentation practices, data integrity aspects, etc.

·Ability to work with digital tools and software applications.

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

·This list could vary based on location/region



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