Materials Scientist [Self Care / Technical Compliance]

Materials Scientist [Self Care / Technical Compliance]

Wat we doen

Bij Kenvue realiseren we de buitengewone kracht van dagelijkse verzorging. Gebouwd op meer dan een eeuw erfgoed en geworteld in de wetenschap, zijn we het huis van iconische merken - waaronder NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® en BAND-AID® die je al kent en waar je van houdt. Wetenschap is onze passie; Zorg is ons talent.

Wie we zijn

Ons wereldwijde team bestaat uit ~ 22.000 briljante mensen met een werkcultuur waar elke stem telt en elke bijdrage wordt gewaardeerd. We zijn gepassioneerd door inzichten, innovatie en toegewijd aan het leveren van de beste producten aan onze klanten. Met expertise en empathie betekent een Kenvuer zijn dat je elke dag de kracht hebt om miljoenen mensen te beïnvloeden. We stellen mensen op de eerste plaats, geven er veel om, verdienen vertrouwen met de wetenschap en lossen op met moed - en hebben schitterende kansen voor je klaarliggen! Geef samen met ons vorm aan onze toekomst - en die van jou. Klik voor meer informatie op here.

Rol rapporteert aan:

GER PESQ E DESENV

Locatie:

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

Werklocatie:

Hybride

Wat je gaat doen

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 
Required Qualifications:
•    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 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.

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

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