CBK655 | Regulatory Affairs Specialist (Fixed Term 12 Months)

CBK655 | Regulatory Affairs Specialist (Fixed Term 12 Months)

21 ene
|
Kenvue
|
Xico

21 ene

Kenvue

Xico

.DescriptionKenvue is currently recruiting for:**Regulatory Affairs Specialist**This position reports into GRA CMC Regulatory Affairs Manager and is based at Mexico City.
**Who we are**At Kenvue, part of the Johnson & Johnson Family of Companies, we believe there is extraordinary power in everyday care.
Built on over a century of heritage and propelled forward by science, our iconic brands—including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® and BAND-AID® —are category leaders trusted by millions of consumers who use our products to improve their daily lives.
Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights,



and a commitment to continually earning a place for our products in consumers' hearts and homes.
**What you will do**Key Responsibilities:- Develop and maintain regulatory strategies and submissions for new products and changes to existing products in alignment with industry standards and regulations.- Collaborate with cross-functional teams to ensure compliance with regulatory requirements throughout the product development lifecycle.- Provide guidance and support to internal stakeholders on regulatory matters, including labeling, advertising, and promotional materials.- Stay up-to-date with changes in regulations and industry standards, and communicate potential impacts to the organization.- Contribute to the development and implementation of quality systems and processes to ensure compliance with regulatory requirements.- Participate in regulatory agency inspections and audits, and assist with the resolution of any findings or observations.- Develop and execute regulatory strategies to ensure compliance with global, regional,



and local regulations and guidelines- Collaborate with cross-functional teams to plan, conduct, and manage regulatory activities to meet department and company objectives- Prepare and compile high-quality regulatory submissions, responses to regulatory agencies questions, and other correspondence in accordance with regulatory agency regulations and guidelines- Review and approve artwork and promotional copy material to ensure regulatory compliance- Provide solutions to complex problems and ensure quality and compliance in all actions- Maintain and archive regulatory documentation in accordance with regulatory agency regulations and guidelines- Present status updates on product/project activities to key internal/external stakeholders- Assist in the development of best practices for Regulatory Affairs processesQualifications**What we are looking for**Required Qualifications

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