Materials Scientist [Self Care / Technical Compliance]

Kenvue Inc.; São José dos Campos; Híbrido; BRL 90 000 - 130 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Competitive total rewards package

Paid holidays/vacation/volunteer time

Learning & Development opportunities

Employee resource groups

Resumo da oferta

Kenvue is seeking a Materials Scientist for Self Care - Technical Compliance to drive analytical deliverables for OTC projects. You will review and write technical documents, ensure data integrity, and lead changes to APIs/excipients under regulatory timelines.

Responsibilities include establishing material specs, supporting API spec justifications, and coordinating cross-functional teams to meet project objectives. Fluent English and strong writing skills are required.

Qualificações

• Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering or related field.
• Minimum 2 years in pharmaceutical industry.
• Strong analytical background with HPLC/UPLC/GC.
• Experience with method validation and method transfer.
• Knowledge of regulations for drug substances method development.
• Fluent in English (written and spoken).
• Excellent communication and collaboration skills.
• Capable of adapting to uncertain environments and changing priorities.

Responsabilidades

• Review analytical documents to support product development and life cycle projects (validation protocols/reports, COAs, raw materials documents) per LATAM/US regulatory requirements.
• Assess and implement API and excipient changes ensuring regulatory and quality standards.
• Establish materials specifications aligned with standards.
• Support justifications for API specifications per international guidelines and local regulations.
• Coordinate technical project activities and ensure timely delivery.
• Write and review protocols, reports, and technical assessments ensuring SOP and regulatory compliance.
• Communicate with regulatory, product development and quality teams.
• Identify process improvements across procedures and systems.
• Ensure data integrity by reviewing raw data and performing statistical evaluations.

Conhecimentos

HPLC

UPLC

GC

Analytical techniques

Method validation

Method transfer

Regulatory knowledge

English fluency

Communication skills

Adaptability

Formação académica

Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering or related field

Descrição da oferta de emprego

Materials Scientist [Self Care / Technical Compliance]

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:

GER PESQ E DESENV

場所:

Latin America, Brazil, Sao Paulo, Sao Jose dos Campos

勤務地:

ハイブリッド

あなたがすること

The Materials Scientist Self Care – Technical Compliance will be responsible to work on analytical deliverables on Self Care (OTC) projects, reviewing and writing technical documents in compliance with standard operating procedures and regulatory requirements ensuring also data integrity. Additionally will lead supplier changes implementation, compendial updates and providing plant support to solve materials issues from internal/external manufacturing plants under restricted timelines. This position will coordinate and execute technical aspects of projects, applying knowledge of analytical chemistry fundamentals to guide raw material analysis, characterization strategies and specification setting. Additionally, the scientist will write and review technical documents, ensuring compliance with standard operating procedures and regulatory requirements.

Key Responsibilities

• Review/elaborate analytical technical documents to support product development and life cycle management projects, including test method validation protocols and reports, certificates of analysis, and other related documents applicable to raw materials, all in accordance with regulatory requirements from LATAM and US health authorities, as well as compliance policies.
• Assess and implement changes to APIs and Excipients, including monographs changes, ensuring regulatory compliance and quality standards are met.
• Establish materials specifications, ensuring they align with industry standards and meet project requirements.
• Support development of justifications for API specifications based on international guidelines and local regulatory requirements, ensuring thorough documentation for audits and reviews.
• Exhibit a sense of urgency in addressing challenges, prioritizating and ensuring timely resolutions to achieve project objectives successfully.
• Communicate clearly with internal teams within Kenvue Self-Care, including Regulatory, Product Development and Quality fostering collaboration and alignment.
• Identify process improvement opportunities to streamline and simplify procedures, documentation and systems.
• Prepare and review comprehensive technical documents, including protocols, reports and and technical assessments. Review analytical raw data to ensure data integrity in the R&D environment. Perform and review statistical evaluations of data from analytical validation studies.

What we are looking for

• Education: minimum Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering or related field is required.
• Minimum experience of 2 year in Pharmaceutical industry is required.
• A strong analytical background in HPLC, UPLC, GC and other analytical techniques is required.
• Experience with method validation, method transfer is required.
• Knowledge about the regulations and/or guidelines related to method development for drug substances is mandatory for this position.
• It is preferred that this candidate have strong technical writing skills.
• Fluent level of English
• Good communication and collaboration skills.
• Person that thrives in uncertain circumstances. Adapt to changes in the work environment; manage multiple tasks and competing demands.

Desired Qualifications

• Experience in implementing technical projects or in site issues support to manufacturing/production area is a differential.
• Familiarity with regulations and guidelines related to method development and validation for drug substances

What’s in it for you

• Annual base salary. This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.
• Competitive Total Rewards Package*
• Paid Company Holidays, Paid Vacation, Volunteer Time & More!
• Learning & Development Opportunities
• Employee Resource Groups
• This list could vary based on location/region

*Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of di

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