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SR SCIENTIST ANALYTICAL LCM


Kenvue Inc


Location

Brasil | Brazil


Job description

Come work at the forefront of science - and help the brands you grew up with grow and evolve into the next generation.

Job Description - SR SCIENTIST ANALYTICAL LCM (2407016841W)

SR SCIENTIST ANALYTICAL LCM - 2407016841W

Description

Kenvue is currently recruiting for:

Senior Scientist Analytical LCM

We are seeking a skilled Senior Scientist of Analytical R&D to lead development for new and existing drug products, manages projects, and authors technical documents. They comply with safety and regulatory requirements, communicate testing status, and perform analytical activities to support ongoing projects.

This position is based at Sao Jose dos Campos.

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 .

What You Will Do

The Senior Scientist Analytical NPD or LCM is responsible for:

Key Responsibilities

· Lead analytical development activities for new drug product development, including pre-formulation studies, method development and validation and stability studies utilizing analytical instrumentation such as HPLC, UPLC, GC, FT-IR, UV, dissolution apparatus, and wet chemistry as applicable.

· In addition to the bench activities, the Senior Scientist, Analytical R&D will be responsible for analytical project management and the independent execution of analytical project deliverables

· Responsible for authoring/reviewing of technical documents such as analytical method development histories, method validation protocols/reports and stability reports in compliance with standard operating procedures and regulatory requirements.

· Comply with company safety practices, as well as operate in compliance with all applicable Federal, State, and local regulations.

· Communicate testing status and perform assigned analytical activities to support on-going projects.

Qualifications

What We Are Looking For

Required Qualifications

· A minimum of a Bachelor's degree and 5 years of analytical chemistry experience OR a Master’s degree and 3 years of analytical chemistry experience OR a Ph.D. is required.A focused degree in Chemistry or Pharmaceutical Chemistry is preferred.

· Experience in the pharmaceutical industry is required.

· Experience with HPLC and/or UPLC is required.

· It is preferred that this candidate have experience performing instrumental and wet chemistry testing including titrations, GC, FT-IR , UV and other chemical analyses successfully.

· Familiarity with GMPs is required.

· Strong technical writing skills and communication skills are required.

· Ability to handle multiple, competing priorities and work with minimal supervision to creatively accomplish technical tasks is required.

What’s In It For You

· Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!

· Learning & Development Opportunities

· Employee Resource Groups

· This list could vary based on location/region

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.

Primary Location

Kenvue is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive considerationfor 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.andEqual Employment Opportunity Posters GINA Supplement.

If you are an individual with a disability, please check ourpage for information on how to request an accommodation.Disability Assistance

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