Principal Scientist - Self-Care R&D

Principal Scientist - Self-Care R&D

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：

Manager, Self Care R&D

位置：

North America, United States, New Jersey, Summit

工作地点：

完全现场

你会做什么

The Principal Scientist, R&D is responsible for delivering against the Self-Care innovation pipeline and serving as a technical lead on product development and new product launches to deliver on unmet consumer needs. Self-Care is considered one of 3 strongholds within Kenvue and contains iconic brands such as TYLNEOL® ZYRTEC®, MOTRIN®, PEPCID®, IMODIUM® and more. The Self-Care segment has high aspirations and expectations to expand the portfolio with product innovation and scientific leadership.  With this expansion comes a need for experienced technical talent who can partner with commercial functions to understand consumer and HCP insights and deliver unparalleled scientific solutions, lead complex technical programs, and begin sharing this knowledge and expertise to help mold the scientists of the future.  We are seeking a highly skilled and experienced Principal Scientist to join our Self-Care R&D team. This role requires a strategic thinker with a strong background in formulation and/or process development, including analyzing new science and consumer insights to help build a strategic innovation pipeline aligned with global brand needs.

Key Responsibilities:

This position will serve as technical lead on cross-functional project teams. They will work with the R&D organization as well as commercial and operations team members to develop and expand the Self Care pipeline as well as downstream product development activities.  Additional responsibilities of this role include the following:

• The Principal Scientist will be accountable for the design and execution of multiple projects concurrently.
• Close collaboration with commercial partners to understand consumer & HCP unmet needs to shape product and claims deliverables.
• Lead the design, formulation, and development of innovative pharmaceutical products, with a focus on solid and liquid dose forms.
• Design and execute strategies to overcome technical challenges in product formulation and manufacturing processes.
• Implement process improvements and troubleshooting to enhance product quality and manufacturing efficiency.
• Collaborate with manufacturing teams to ensure seamless technology transfer from R&D to production.
• Ensure compliance with FDA regulations and GxP standards throughout the development process.
• Collaborate with regulatory affairs to ensure support FDA filings such as NDA, ANDA, 510K, RFD, etc., ensuring all documentation and data meet regulatory requirements.
• Stay current with regulatory guidelines and industry standards to ensure compliance and best practices.
• Develop and manage project timelines, budgets, and resources to ensure successful project execution.
• Communicate complex scientific and technical information effectively to both technical and non-technical stakeholders.
• Mentor and develop future talent through direct and indirect guidance by foster a culture of collaboration and teamwork within the department.
• Review external literature, data sources and intellectual property to stay current and assess competitive threats, identify new trends and opportunities to drive growth.
• The Principal Scientist may draft and execute peer reviewed manuscripts, technical reports and communications and patent fillings as appropriate

• Influence and lead cross-functional teams through technical expertise and strategic vision.

What we are looking for
Required Qualifications:

• Bachelor’s Degree with 6+ years or Master's Degree with 5+ years, or Ph.D. with 3+ years of relevant experience. Degree must be in Chemistry, Pharmaceutical Sciences, Chemical Engineering, Materials Engineering, Biomedical Engineering, Biophysics, or a related field.
• Experience in product or process development within the consumer health care or pharmaceutical industry. Experience in late-stage development and commercialization is highly desirable.
• Proficiency in formulation development, process optimization, and/or analytical techniques. Experience with QbD (Quality by Design) principles is a plus.
• Knowledge and experience with regulatory requirements including ICH, FDA, compendia (e.g. USP, JP, EP, etc.) is highly preferred.
• Proven track record of managing complex projects, with strong organizational and leadership skills. Excellent project management skills, including timeline management, budget oversight, and team coordination.
• Flexibility in schedule to support global teams and willingness to travel up to 25% domestically and internationally.

Desired Qualifications:

• Proven experience in solid dose formulation and manufacturing (tablets, capsules, etc).
• Proven experience in formulation of liquid and semi-solids for topical and/or nasal application.
• Experience in supporting FDA filings such as NDA, PAS, ANDA, 510K, RFD, etc.
• Demonstrated leadership by influence and ability to mentor and develop team members.
• Foundational understanding of FDA regulations and guidelines for pharmaceutical product development.

对您有什么好处

$127,075.00 - $179,400.00

这考虑了许多因素，包括工作地点、候选人的技能、经验、教育水平和其他与工作相关的因素

Kenvue 很自豪能成为一个机会均等的雇主。所有合格的申请人都将根据业绩获得就业考虑，不分种族、肤色、宗教、性别、性取向、性别认同、年龄、国籍或受保护的退伍军人身份，并且不会因残疾而受到歧视。