Senior Scientist- Self Care

Kenvueは現在、a: Senior Scientist- Self Care

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 Role reports to:

RES. MANAGER ORAL DRUG DELIVERY TECH.

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

Self-Care is a core strength for Kenvue with ambitious goals to grow the portfolio through product innovation and scientific leadership in priority markets. To support this growth, we need experienced technical talent who can deliver strong science, lead complex programs, and help develop the next generation of scientists. We are seeking a highly skilled Senior Scientist to join our Self-Care Future of Kenvue Innovation team. This role requires a strategic thinker with strong formulation and/or process development expertise who can lead and execute R&D projects focused on creating and optimizing self-care solutions. The successful candidate will manage multiple projects, solve complex technical challenges, and help shape the strategic direction of our R&D efforts. This role requires a high degree of autonomy and collaboration in a fast-paced, regulated environment. Key Responsibilities: Lead the design, formulation, and development of innovative self-care products, with a focus on solid, semi-solid and liquid dose forms. Design and execute strategies to overcome technical challenges in product formulation and manufacturing processes. Collaborate with product development and technical teams to ensure seamless technology transfer. Ensure compliance with FDA regulations and GxP standards throughout the development process. Stay current with regulatory guidelines and industry standards to ensure compliance and best practices. Utilize fundamental project management skills to track progress, mitigate risks, and deliver results. Communicate complex scientific and technical information effectively to both technical and non-technical stakeholders. Participate in initiatives such as patent reviews, scientific forums, and safety leadership programs. Shape the scientific strategic planning and decision-making processes related to product development and portfolio management, aligning R&D activities with broader business objectives. Demonstrate business acumen by understanding the impact of R&D activities on the company's overall goals. What we are looking for Required Qualifications: Bachelor’s Degree with 5+ years or Master’s degree with 3+ years of relevant experience. Degree must be in Materials Science, Biomedical Engineering, Pharmaceutical Sciences, Chemical Engineering, Chemistry, or a related discipline. Experience in early-stage product development within the consumer health care or pharmaceutical industry . Proficiency in formulation development, process optimization, and/or analytical techniques. Experience with QbD (Quality by Design) principles is required. Experience in typical unit operations such as granulation, roller compaction, drying, milling, blending, compression/encapsulation, film coating, and spray drying etc. 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, 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 and liquid dose formulation and manufacturing (tablets, capsules, soft chews, gummies). Proven experience in formulation of liquid and semi-solids for topical, oral and/or nasal applications. 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

このポジションの新入社員の年間基本給の範囲:

$105,400.00 - $148,800.00 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.

競争力のある福利厚生パッケージ*

有給の会社の休日、 有給休暇、ボランティアタイム&詳細!

学習&開発の機会

Kenvuer Impact Networks

このリストは場所/地域によって異なる場合があります

*注:Kenvueの合計報酬には、給与、ボーナス(該当する場合)、および福利厚生が含まれます。あなたのタレントアクセスパートナーは、採用および採用中に、関連する場所の報酬提供総額と特定の給与範囲について詳しく共有することができます。採用プロセス. Kenvueは機会均等雇用者であることを誇りに思っています。人種、肌の色、宗教、性別、性的指向、性同一性、年齢、出身国、または保護された退役軍人の地位に関係なく、すべての資格のある応募者は、能力に基づいて雇用の検討を受け、障害に基づいて差別されることはありません。

障害を持つ個人の方は、宿泊施設のリクエスト方法について、私たちの障害者支援ページを確認してください。

#J-18808-Ljbffr Kenvue Inc.