Principal Scientist - Self-Care R&D

Principal Scientist - Self-Care R&D

私たちがしていること

Kenvueで、日常のケアの並外れた力を実感します。100年以上にわたる伝統を基盤に、科学に根ざした当ホテルは、ニュートロジーナ®、アヴェーノ®、タイレノール®、リステリン®、ジョンソンズ®、バンドエイド®など、すでにお馴染みのアイコニックなブランドを展開しています。科学は私たちの情熱です。ケアは私たちの才能です.

Who We Are

私たちのグローバルチームは~22,000人の優秀な人々で、すべての声が重要で、すべての貢献が評価される職場文化を持っています。 私たちは洞察に情熱を注いでいます。 革新とお客様に最高の製品を提供することに取り組んでいます。専門知識と共感力を持つKenvuerであることは、毎日何百万人もの人々に影響を与える力を持つことを意味します。私たちは人を第一に考え、熱心に気を配り、科学で信頼を勝ち取り、勇気を持って解決します。そして、素晴らしい機会があなたを待っています!私たちと一緒に、私たちの、そしてあなたの未来を形作りましょう。詳細についてはをクリックしてくださいhere.

Role reports to:

Manager, Self Care R&D

Location:

North America, United States, New Jersey, Summit

勤務地:

フルオンサイト

あなたがすること

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.

それは何ですか

$127,075.00 - $179,400.00

これは、勤務地、候補者のスキル、経験、教育レベルなど、多くの要素を考慮に入れています。その他の仕事関連の要因.

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