QA/QC Technical Writer

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在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。

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我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.

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你會做什麼

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.

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