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Scientist - R&D Materials

Función del trabajo:
Fecha de publicación:
Fecha de finalización:
ID:
2607048208W

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Scientist - R&D Materials

Lo que hacemos

En Kenvue, nos damos cuenta del extraordinario poder del cuidado diario. Sobre la base de más de un siglo de herencia y arraigados en la ciencia, somos el hogar de marcas icónicas, incluidas NEUTROGENA®, AVEENO,® TYLENOL,® LISTERINE,® JOHNSON'S® y BAND-AID® que ya conoces y amas. La ciencia es nuestra pasión; El cuidado es nuestro talento.

Quiénes somos

Nuestro equipo global está formado por ~ 22.000 personas brillantes con una cultura laboral en la que cada voz importa y cada contribución es apreciada. Nos apasionan las ideas, innovación y comprometidos con la entrega de los mejores productos a nuestros clientes. Con experiencia y empatía, ser un Kenvuer significa tener el poder de impactar a millones de personas todos los días. Ponemos a las personas en primer lugar, nos preocupamos ferozmente, nos ganamos la confianza de la ciencia y resolvemos con coraje, ¡y tenemos oportunidades brillantes esperándote! Únase a nosotros para dar forma a nuestro futuro y al suyo. Para obtener más información, haga clic en aquí.

Role reports to:

Principal Scientist, R&D Materials Analytical

Ubicación:

Asia Pacific, India, Maharashtra, Greater Mumbai

Lugar de trabajo:

Totalmente in situ

What will you

Scientist R&D Materials

Roles and Responsibilities:

1.      To provide technical assessment of Raw materials/Products used at Internal and External Manufacturing sites to ensure alignment with current compendia, industry standards, product registrations, and internal procedures.

2.      To liaison between Global sites and Specification team by collaborating with business partners and stakeholders (Internal/External Manufacturing sites, Regulatory, Source Quality, Business Quality, Product team) to gather necessary information to process the spec request.

3.      To ensure compliance with upcoming versions of Pharmacopeia monographs and identifying affected changes to the impacted sites to ensure compliance, prior to its effective date.

4.      To have effective communication skills, for consistent, frequent collaborations with global sites, project team, and outsourced technical writers, via virtual meetings and mail correspondences.

5.      To follow team’s existing processes to ensure completeness, consistency, and accuracy, while finding opportunities and recommending solutions to improve timeliness of the Global Specification request.

6.      To have strategic and operations skills to prioritize and execute project based on business and compliance needs. Partnership and sense of urgency are required to meet the target dates of both global and regional initiatives.

7.      To become an expert in Standard Operating Procedure as well as provide feedback to necessary standard operating procedure owners to ensure procedure reflect business practices.

8.      Demonstrate clear engagement for action on priorities and get the projects targets demonstrating a great sense of urgency.

9.      Flexibility to lead with implementation changes according to new alignments or business need.

10.  Often participate of cross-functional project teams and communicative skills to discuss with different areas (business partners and off-shore technical writers)

11.  Approve specifications and change controls and drive to completion.

12.  Write and/or coordinate specifications and/or change control and guarantee written on time and right the first time.

13. To review the relevant documents / protocols / reports (including but not limited to Material Analytical Report - MAR)

 

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