Kenvue 目前正在招聘 a：
我们做什么
在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。
我们是谁
我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.
Role reports to：
GER TECN PESQ E DESENV位置：
Latin America, Brazil, Sao Paulo, Sao Jose dos Campos工作地点：
混合你会做什么
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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