Commercial Quality Analyst - Fixed Term Contract

Description

Who We Are

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® Brand Adhesive Bandages that you already know and love.

Science is our passion; care is our talent.

Our global team is made up of ~ 22,000 diverse and brilliant people, 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 the life of 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 .

What You Will Do

The position is responsible for:

• The Commercial Quality (CQ) Specialist is responsible for implementation and maintenance of the appropriate Quality Standards and Systems for the operation of the Portuguese Consumer Health organization.

It will also be responsible for partnering with the Portugal Business Head and Management in quality questions & issues and liaison with multiple Quality organizations to drive timely resolution of Quality related issues.

• This position reports to CQ Iberian Head.

It will also support the Southern European Cluster team in defining and implementing departmental strategies and services to optimize and harmonize processes and find opportunities to collaborate in the Cluster and Region!

• The CQ Specialist Portugal will act as a back-up to the Technical Director role, acting as Responsible Person backup for medicines and technical responsible for cosmetics distributed by Johnson & Johnson Portugal and point of contact backup with Health Authorities.

Key Responsibilities

• Responsible for ensuring that all local or Cluster Standard Operating Procedures (SOPs) that describe all GxP related processes are established ensuring adequacy and continuous improvement of Kenvue Quality Management System (QMS)

• Responsible for on time quality review and approval of products marketed in the local markets

• Ensuring that any changes with GxP impact, affecting products or the distribution related activities, are appropriately controlled and supervised.

• Ensuring that a document and data management system is accurately implemented according to internal and local regulatory requirements.

Ensure documents and records are complete, accurate and documented/archived according to written procedures and cGMP requirements.

• Executing Investigations and Root Cause Analysis on time closure.


* Performs review, trending, tracking and monitoring of cGMP processes, procedures, training, documents and records, including but not limited to non-conformance records, change control, and corrective actions / preventive actions (CAPA), complaint...