Senior Specialist-R&D Q&C

Senior Specialist-R&D Q&C

Что мы делаем

At Kenvue, мы осознаем необычайную силу повседневной заботы. Основанный на более чем вековом наследии и уходящий корнями в науку, мы являемся домом культовых брендов, включая NEUTROGENA®, AVEENO,® TYLENOL,® LISTERINE,® JOHNSON'S® и BAND-AID®, которые вы уже знаете и любите. Наука – наша страсть; забота – это наш талант.

Кто мы

Наша глобальная команда – это ~ 22 000 блестящих людей с культурой рабочего места, где каждый голос имеет значение, а каждый вклад ценится. Мы увлечены идеями, инновации и стремление поставлять нашим клиентам лучшие продукты. Обладая опытом и эмпатией, быть Kenvuer означает иметь возможность влиять на миллионы людей каждый день. Мы ставим людей на первое место, заботимся о настолько, завоевываем доверие наукой и смело решаем – и вас ждут блестящие возможности! Присоединяйтесь к нам, чтобы формировать наше будущее и ваше. Для получения дополнительной информации, нажмите here.

Role reports to:

Manager, R&D Q&C

Местонахождение:

Asia Pacific, India, Maharashtra, Greater Mumbai

Место работы:

Гибрид

Что ты будешь делать

Kenvue is currently recruiting for:

               

Senior Specialist-R&D Q&C

This position reports into Manager-R&D Q&C and is based at Mumbai.

What we do

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who we are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours. For more information, click here.

               

Role reports to: Manager-R&D Q&C

Location: Mumbai

What you will do

• The Senior Specialist-R&D Q&C is responsible for review of documents which includes but not limited to Procedures, laboratory non-conformances, change controls, Investigations, CAPA reports, test methods, validation protocol and reports, instrument qualification documents, computerized system validation documents, stability protocols and reports, method transfer protocols and reports, technical justifications, providing coaching and training to employees, leading compliance risk identification, and ensuring adherence to quality agreements and compliance requirements:

Key Responsibilities

• Lead and manage research and development quality & compliance processes to ensure product quality and compliance with regulatory standards.
• Collaborate with cross-functional teams to drive continuous improvement initiatives and enhance R&D procedures.
• Conduct thorough analysis of R&D data to identify trends and areas for improvement
• Provide guidance and mentorship to junior Q&C  specialists to foster professional development and growth.
• Collaborate with cross-functional teams to ensure investigations are in compliance with quality assurance standards and regulations.
• Lead and support the facility in identifying and eliminating compliance risks related to non-conformance investigations and quality systems.
• Provide coaching and training to employees on quality assurance procedures and best practices
• Supplier Qualification & monitoring to ensure compliance with Regulations, Kenvue standards, quality agreements and specifications
• Continuously discover, evaluate, and implement new technologies to enhance quality assurance processes.
• Deployment of Quality Management Systems transformation for R&D Mumbai.
• End to end compliance of analytical and microbiology R&D laboratories.
• Conduct or co-ordinate site’s Internal Audits/Surprise checks and supplier audits, prepare quality agreements with suppliers as and when required.

 What we are looking for

Required Qualifications

Master’s Degree in Science (M.Sc Microbiology/ Chemistry).

• Proven working experience in quality assurance and compliance within a manufacturing or laboratory setting (Minimum 12 years’ experience)
• Must have  Auditor Certifications (Lead Auditor) & experience in Qualification of Suppliers.
• Knowledge of good manufacturing practices and good laboratory practices.
• Must have faced audits like USFDA, EU GMP, WHO etc.
• Governance of suppliers, distributors, contract laboratories and external manufacturers..
• Experience of project management including planning, leading, coordinating and execution of the projects.
• Must have experience in developing/implementing/testing automations like Electronic Document Management, Learning Management Systems, Quality Management System, laboratory Information Management System.
• Experience in Quality & Compliance of NPD/NPI from development stage to commercialization.

 Desired Qualifications

• Strong knowledge of regulatory standards and quality & compliance best practices
• Experience with quality assurance procedures and best practices
• Strong attention to detail and ability to identify compliance risks
• Excellent communication and leadership skills to effectively collaborate with cross-functional teams
• Excellent communication and leadership skills to provide coaching and training to employees

 What’s in it for you

• Competitive Benefit Package*        
• Paid Company Holidays, Paid Vacation, Volunteer Time & More!        
• Learning & Development Opportunities        
• Kenvuer Impact Networks        
• 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.

       

Если вы являетесь человеком с ограниченными возможностями, пожалуйста, ознакомьтесь с нашим страница помощи инвалидам для получения информации о том, как запросить приспособление.