Senior Scientist

Senior Scientist

Ce que nous faisons

Chez Kenvue, nous réalisons le pouvoir extraordinaire des soins quotidiens. S'appuyant sur plus d'un siècle d'héritage et enraciné dans la science, nous sommes la maison de marques emblématiques - dont NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® et BAND-AID® que vous connaissez et aimez déjà. La science est notre passion ; Le soin est notre talent.

Qui nous sommes

Notre équipe mondiale est composée de ~ 22 000 personnes brillantes avec une culture d'entreprise où chaque voix compte et chaque contribution est appréciée. Nous sommes passionnés par les idées, l'innovation et l'engagement à fournir les meilleurs produits à nos clients. Avec de l'expertise et de l'empathie, être un Kenvuer signifie avoir le pouvoir d'avoir un impact sur des millions de personnes chaque jour. Nous donnons la priorité aux personnes, nous nous soucions farouchement, nous gagnons la confiance grâce à la science et nous résolvons les problèmes avec courage - et nous vous offrons de brillantes opportunités ! Joignez-vous à nous pour façonner notre avenir et le vôtre. Pour plus d'informations, cliquez sur ici.

Role relève à :

Global API Synthesis Manager

Lieu :

Asia Pacific, India, Maharashtra, Greater Mumbai

Lieu de travail :

Hybride

Ce que tu vas faire

Senior Scientist R&D Materials

This position reports into Manager and is based at Mumbai, India.

What will you do 

Senior Scientist RMC (R&D) is responsible for supporting Change Management processes within the Asia Pacific Region (APAC) and supporting global base business operations as needed, specifically as it relates to supplier driven changes and troubleshooting for internal and external manufacturing sites.  This position works closely with global business partners to deliver some global initiatives.  

The Senior Scientist RMC (R&D) will collaborate with a group of technical professionals to manage and provide technical guidance on raw material projects for existing marketed products including, Over the Counter (OTC) monograph drug products, New Drug Applications (NDA) and Class II Medical Device products in the Consumer portfolio. The portfolio includes brands such as TYLENOL®, MOTRIN®, BENADRYL ®, NICORETTE ®, ZYRTEC®, IMODIUM ®, CALPOL®, and SUDAFED ®

Key Responsibilities:  

As a Senior Scientist at APAC Materials, this role is characterized by a diverse and impactful set of responsibilities:  

• Drive the execution of raw material qualification projects for cost improvement projects, raw material discontinuations, and supplier driven changes. This is achieved through close collaboration with the Global Materials team, R&D and key stakeholders like Source, Quality, Tech Ops.  
• Ensure smooth execution of Business Continuity project, support for Raw Material & API related investigations, Supplier issues, Documentations and other API related assessment following internal SOPs.  
• Shall possess synthetic chemistry experience and conduct thorough assessments of the impact of raw material changes on formulations across the spectrum of Self-Care & other categories.
• Perform in-depth review of DMF and RM characterization (HPLC, DSC, mass spectrometry, FTIR, and others).  
• Meticulously document change control and related activities in various systems, adhering to defined processes with a commitment to compliance.  
• Craft compelling technical justifications, reports, and summaries based on robust scientific experimentation and rationale, ensuring harmonization with project leads. 
• Focus on driving science-based problem solving and identify improvement opportunities
• Cultivate strong collaboration with cross-functional teams, including R&D formulators and Tech Ops Scientists, to facilitate seamless communication and ensure the timely sharing of qualification data before implementing raw material changes in both internal and external manufacturing sites.  
• Lead independently to make a detailed execution plan & coordinate with key stakeholders to ensure our products can comply with the latest regulation requirements timely, following changes in the current regulatory requirements. 
• To contribute to the areas which lack a standardized process in daily work. 
• To proactively connect with global key stakeholders, to improve the APAC process through learning from other’s strengths and offsetting their own weaknesses. 
• Participate in multi-functional teams to understand problems, support investigations, implement resolution, and develop optimized processes

What we are looking for

Required Qualifications

• Minimum of Master’s Degree in Chemistry /Pharmacy/Life Science with 7-10 years of experience OR a PhD with 5 years of experience

Desired Qualifications

• Experience in the Pharmaceutical Industry is required.
• Experience in the scale-up, manufacturing and plant troubleshooting of API or Solid & or Liquid Dose OTC/ NDA/ Pharmaceutical products is required
• Experience in Synthesis or manufacturing of API’s or pharmaceutical products is strongly preferred
• Strong technical expertise in raw materials, synthesis and a comprehensive understanding of their impact on Over the Counter (OTC) and New Drug Application (NDA) formulations is highly preferred.
• Deep understanding of standard methodologies and procedures that apply to the support of marketed products locally and globally is preferred
• A deep understanding of GxPs is required

What’s In It For You

• Competitive Benefit Package
• Learning & Development Opportunities
• Employee Resource Groups 
• This list could vary based on location/region.

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 identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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