QA/QC Technical Writer

QA/QC Technical Writer

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:

Site Quality and Compliance Lead

Местонахождение:

Europe/Middle East/Africa, South Africa, Gauteng, Johannesburg

Место работы:

Гибрид

Что ты будешь делать

Kenvue is currently recruiting for:

QA/QC Technical Writer

This position reports into Quality & Compliance Lead and is based in Cape Town, South Africa.

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®, 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: Quality & Compliance Lead

Location: Cape Town, South Africa

Travel %: Minimal

Pay: 24

What you will do

•The QC / QA Technical Writer is responsible for gathering, organizing, and verifying technical information, developing and editing documents, and ensuring specifications meet established standards.

•You will also participate in all lifecycle management projects on site and be part of audit readiness team activities.

Key Responsibilities

Key Responsibilities include:

• Compiles and maintains technical information for the Quality Control Laboratory and Quality Assurance, which includes pertinent information for product registration submission for new and existing products, in compliance with corporate and regulatory requirements.
• Manages the updating of analytical specifications and procedures for new and existing raw materials, bulk and finished product, as well as packaging components using the latest regulatory, pharmacopoeia, Kenvue and Industry Guidelines.
• Reviews and approves Artwork as the Quality Assurance designee generated for products manufactured at Kenvue SA (Pty) Ltd and external contract manufacturers, where required.
• Manages master quality assurance documentation including oversight of manufacturing and packaging batch record updates and revision history.
• Maintaining analytical reports on the electronic lab information system, to ensure that test results can be captured and trended for investigational and product quality review purposes.
• Maintenance of product history for raw materials, finished products, packaging components and artwork.

What we are looking for

Required Qualifications 

• Minimum 4 years of experience in documentation and chemistry in a laboratory environment.
• Education: Bachelor’s degree in chemistry or equivalent degree in Science.
• Prior working experience as a technical writer is a must, preferably from a Pharma company.
• Experience in review and approving Artwork, as the Quality Assurance designee, generated for products manufactured and external contract manufacturers, where required.
• Excellent communication skills and computer proficiency
• Compliance oriented and attention to detail
• Ability to work with cross-functional teams and cross-cultural organizations

What’s in it for you

• Competitive Benefit Package
• Learning & Development Opportunities
• Kenvuer Impact Networks
• 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 based on merit 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.

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