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在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。
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我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.
Role reports to：
GER TECN PESQ E DESENV位置：
Latin America, Brazil, Sao Paulo, Sao Jose dos Campos工作地點：
混合你會做什麼
This individual will lead the strategy and execution of analytical deliverables on North America Self Care (OTC) projects. This includes defining the analytical strategy, execution planning, timing, resource requirements and interdependencies to complete the project deliverables. The Scientist II, R&D Analytical is responsible for performing chemical analysis, conducting research programs, and developing research proposals to meet exploratory objectives in product discovery:
Key Responsibilities
Lead and manage analytical research projects in R&D department focused on launching new products and support the Kenvue´s product pipeline according to FDA and Health Canada Authorities
Validate and transfer analytical methods to support product development and life cycle management projects
Collaborate with cross-functional teams to drive scientific advancements
Provide technical expertise in analytical instrumentation and data analysis
Stay current with industry trends and technologies to drive innovation
Execute analytical test evaluations and analyses and other projects
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 validation, transfer and stability studies or other related documents applied to drug products.
Support investigations due to analytical validation, transfer and stability studies.
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.
What we are looking for
Required Qualifications
A minimum of a bachelor’s degree in Chemistry, Chemistry Engineering or Pharmaceutical Chemistry.
Solid experience in the pharmaceutical industry in R&D Analytical
A strong analytical background in HPLC, UPLC, GC, dissolution and other analytical techniques is required.
Experience with method validation and method transfer is required.
Experience with stability studies is required.
Solid understanding of analytical and physical testing capabilities
Strong analytical and problem-solving skills.
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.
Excellent verbal and written communication abilities.
Advanced level of English is required for this position (oral for active participation in global meetings and written communication).
Desired Qualifications
Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health environment
Excellent communication and collaboration skills
Experience with Empower chromatography data system, using electronic laboratory notebooks (ELN), and LIMS systems.
It is preferred that this candidate has strong technical writing skills and project management skills.
Intermediate level of Spanish can be considered a differential.
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