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addressEndereçoSão José dos Campos, SP
CategoriaPesquisa e ciência

Descrição do trabalho

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 – R&D Analytical – Self Care (OTC) (2307015366W)

Sr. Scientist – R&D Analytical – Self Care (OTC) - 2307015366W

Description

Kenvue is currently recruiting for:

Sr. Scientist – R&D Analytical - Self Care (OTC)

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.

What You Will Do

Kenvue is recruiting a Senior Scientist, R&D Analytical to be based in São José dos Campos, Brazil.This individual will lead the strategy and execution of analytical deliverables on regional Self Care (OTC) projects. This includes defining the analytical strategy, execution planning, timing, resource requirements and interdependencies to complete the project deliverables.

This individual will write and review technical documents including analytical method assessments, method validation / transfer protocols, and reports in compliance with standard operating procedures and regulatory requirements.

Key Responsibilities

· Subject Matter Expert (SME) for a pool of new products development and new products introduction in LATAM markets from R&D Analytical standpoint

· Communicate clearly with the internal organization and with the global teams in forums related to projects from strategy definition to project execution.

· Collaborate effectively with project members following priorities, checkpoints and timelines to guarantee project milestones.

· Write technical documents to support product registration, quality and compliance policies – protocols and reports related to test method development, test method validation, stability studies and other related documents applied to raw materials and drug products.

· Support investigations due to product development stage and support appropriate answer to deficiency letters from Health Authorities on the dossiers submitted.

· Lead complexity and to work collaboratively in partnership with analytical areas in the globe to leverage existing studies and knowledge generated in other sites of the organization.

· Find opportunities to improve processes or project timelines when appropriate.

· Communicate effectively analytical leadership on issues which require escalation.

Qualifications

What We Are Looking For

Required Qualifications

· Education: A minimum of a bachelor’s degree in chemistry, Chemistry Engineering or Pharmaceutical Chemistry.

· At least 3 years of experience in the pharmaceutical industry in R&D Analytical

· A strong analytical background in HPLC, UPLC, GC and other analytical techniques is required. Experience with advanced chemistry will be considered as a differential.

· Experience with method validation and method transfer is required.

· Experience with stability studies according to regional regulations is required.

· It is preferred that this candidate have experience performing/ evaluating statistical analysis of the analytical studies conducted.

· Knowledge about the regulations and/or guidelines related to method development & validation for drug products, drug substance is mandatory for this position.

· It is preferred that this candidate have strong technical writing skills and project management skills.

· Advanced level of English is required for this position (oral for active participation in global meetings and written communication).

· Intermediate or higher levels of Spanish can be considered a differential.

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 identify, 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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Refer code: 1456647. Kenvue - O dia anterior - 2024-02-05 13:02

Kenvue

São José dos Campos, SP
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