Principal Scientist - Self-Care R&D

我們做什麼

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。

我們是誰

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.

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你會做什麼

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.

對您有什麼好處

這考慮了許多因素，包括工作地點、候選人的技能、經驗、教育水準和其他與工作相關的因素

Kenvue 很自豪能成為一個機會均等的雇主。所有合格的申請人都將根據業績獲得就業考慮，不分種族、膚色、宗教、性別、性取向、性別認同、年齡、國籍或受保護的退伍軍人身份，並且不會因殘疾而受到歧視。