Associate Scientist

4 weeks ago

Mumbai, India Kenvue Full time

**Associate Scientist**-2307009641W

Description

Kenvue, part of the Johnson & Johnson Family of Companies (Kenvue), is currently recruiting for:
**ASSOCIATE SCIENTIST, ANALYTICAL CHEMISTRY**

This position reports into Deliver Retail Officer and is based in Paranaque.

**Who we are**

At **Kenvue**, part of the Johnson & Johnson Family of Companies, we believe there is extraordinary power in everyday care. Built on over a century of heritage and propelled forward by science, our iconic brands—including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® —are category leaders trusted by millions of consumers who use our products to improve their daily lives. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes. What will you do

**What will you do**

The objective of this position is to deliver analytical services to various Johnson and Johnson 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

**Purpose Of Position**

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.

**KEY RESPONSIBILITIES**

**ANALYTICAL DETERMINATIONS AND TECHNICAL ASSESSMENTS**:

- Ensure qualification on assigned analytical technologies and instrumentation for testing capabilities.
- 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.

**Qualifications**:
**What we are looking for**

**Qualifications And Functional Competencies**:
**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.

**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 and Quality environment preferred

**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 identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability

Primary Location Asia Pacific-India-Maharashtra-Greater Mumbai

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