Junior Commercial Quality Specialist

Junior Commercial Quality Specialist

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 Commercial Quality BNL

Location:

Europe/Middle East/Africa, Czechia, Prague, Prague

Work Location:

Hybrid

What you will do

The Junior Commercial Quality Specialist is responsible for supporting the CQ Manager(s) / CQ Lead(s) to maintain and improve compliance with Quality Management Systems (QMS) across different legal entities within the Central Europe Cluster; more specifically within the BenAlp (BE/NL/LU/AT/CH) and Central Eastern Europe (CZ/SK/HU) subclusters. 

These activities include overseeing the operational aspects of these quality systems, ensuring quality standards are implemented and maintained for Kenvue’s operations. The person will fulfill a key role as main administrative support for the associates acting as different regulated functions (GDP RPs / QPs) & in executing delegated tasks by these functions, across the multiple countries in scope.

Key Responsibilities

• Execution of controls and preparation of (administrative) release of finished medicinal products (evaluation of inbound documentation, transportation temperature checks, administrative checks etc.)

• Assure compliance with local legislation, especially GMP and GDP (BENELUX, CH, AT)

• Evaluation of return documentation to support product disposition decisions of the QPs/RPs

• Support in the supplier qualification and customer qualification processes

• Execution of TopCat approvals (masterdata setup for new codes)

• Execution of Finished Product Specification approvals

• Perform First Article Inspection (FAI) for OTC and medical samples for the countries in scope

• General and broad administrative support (eg. Initiation phase) with regards to key Quality processes such as change control management, investigation / nonconformance management, audit and inspection management, (mock)field action management, etc.

• Act as qualified internal auditor to support the cluster/regional internal audit program

What We Are Looking For

• A trusted colleague to become a partner for the local businesses and mgmt. of the different legal entities across the different subclusters

• An associate that ensures that in every business decision and process, potential quality and compliance impact is assessed and respected

• An agile and passionate talent, keen to learn continuously

Required Qualifications

• A Bachelor’s degree (or equivalent) in a relevant field

• Excellent knowledge of the English language

Essential skills and core competencies

• Knowledge of Microsoft Office software: Excel, Word, PowerPoint, Acrobat

• Good communicator and team player

• Accurate

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.