Senior Scientist, Research & Development [Self Care]

Kenvue; São José dos Campos; On-site; BRL 200,000 - 320,000; Full time

Benefits offered by this job

競争力のある福利厚生

有給休暇制度

学習・開発の機会

Job summary

Kenvueはバリデーション済みの分析手法を活用し、開発中の製品の探索段階を支えるSenior Scientist, R&D Analyticalを募集しています。FDA/Health Canada準拠のプロジェクトを推進し、グローバルチームと連携して新製品の分析開発をリードします。

本ポジションはブラジル・サンパウロ州のオンサイト勤務で、分析機器・データ解析・統計的手法に熟練した方を求めます。英語力が高く、複雑な技術文書の作成能力が必須です。

Qualifications

• 薬物製剤向け分析開発・検証の経験が必須。
• HPLC/UPLC/GC等の分離分析に関する高度な経験。
• 分析法の検証・転送・安定性試験の実務経験が必須。
• 薬物製剤規制のガイドライン知識が望ましい。
• 英語での技術文書作成能力が望ましい。

Responsibilities

• 分析研究プロジェクトを主導・管理し、薬剤開発を支援する。
• 分析法検証・転送を推進し、製品ライフサイクルをサポートする。
• 多部門と連携して科学的進展を推進する。
• 分析機器とデータ解析の専門知識を提供する。
• グローバル会議での戦略定義から実行まで関係者へ伝達する。
• 試験法の検証・転送・安定性試験に関する技術文書を作成する。
• 他サイトと協調して研究成果を活用し、プロジェクト日程を遵守する。

Skills

HPLC/UPLC/GC

分析法検証

安定性試験

統計解析

高度な英語

規制知識

Education

Chemistry/Pharmaceutical Chemistry 学士

Tools

Empower chromatography data system

ELN/LIMS

Job description

Senior Scientist, Research & Development [Self Care]

Kenvueは現在、以下求人を募集しております。

私たちがしていること

私たちKenvueは、日々のケアが持つ驚くべき力を信じています。100年以上の伝統と科学に根ざし、Neutrogena®, Aveeno®, Tylenol®, Listerine®, Johnson’s® and BAND-AID®など、皆様が既にご存じでご愛用いただいているアイコニックなブランドを提供しています。科学は私たちの情熱であり、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、インサイトとイノベーションに情熱を注ぎ、最高の製品をお客様にお届けすることに全力を注ぐ、多様で優秀な22,000人以上の社員で構成されています。専門知識と共感力を備えたKenvuerであることは、毎日何百万人もの人々の生活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、全身全霊をもってケアし、サイエンスで信頼を獲得し、勇気をもって解決します。私たちとあなた自身の未来を、共に切り開いていきましょう。

Role reports to:

GER TECN PESQ E DESENV

場所:

Latin America, Brazil, Sao Paulo, Sao Jose dos Campos

勤務地:

フルオンサイト

あなたがすること

The Senior Scientist, R&D Analytical is responsible for performing chemical analysis, providing guidance to staff, conducting advanced 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
• Lead and oversee chemical analyses to support product discovery objectives
• Provide expert guidance to staff members on 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.
• Lead complexity and to 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 advanced chemistry will be considered as a differential.
• 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.
• It is preferred that this candidate have 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.
• It is preferred that this candidate have strong technical writing skills and project management skills.
• 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
• Strong experience with Empower chromatography data system, using electronic laboratory notebooks (ELN), and LIMS systems.
• Intermediate or higher levels of Spanish can be considered a differential.

What’s in it for you

• Competitive Benefit Package*
• Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!
• Learning & Development Opportunities
• Employee Resource Groups
• This list could vary based on location/region

*Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

障害のある個人の方は、宿泊施設のリクエスト方法について障害支援ページを確認してください。