Sr. Analyst, Quality Systems & Compliance (Projects) Fixed Term – 9 Months

Description

Kenvue is currently recruiting for:

Sr.

Analyst, Quality Systems & Compliance (Projects)

Fixed term - 9 months

months

This position reports into Quality structure based at Kenvue SJC, BRAZIL site.

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® that you already know and love.

Science is our passion; care is our talent.

Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers.

With expertise and empathy, being a Kenvuer means to have the power to impact 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 Quality analyst will be responsible for delivering quality plans across the region in order to achieve projects of the company related to Quality Management system update to new company strategy including system updates, performance metrics, supplier management, quality management system adequacy, product label & codes change, specification, documentation updates including change contro.l

Key Responsibilities

• Participation on quality projects related to regional and global strategic initiatives

• Build collaboration across different functional areas with business partners

• Deliver the Final Project Objectives

• Develop and execute Project plans through collaboration with cross functional team members

• Collaborate with quality functions to meet project deliverables following quality requirements.

• Change control opening and management to track aapplicable GxP related activities on-time and in compliance with Kenvue procedures and country-specific quality/regulatory requirements

• Identify risks effectively and assist in identification and implementation of mitigation plans.

What We Are Looking For

Required Qualifications

• Bachelor's degree in pharmacy, chemical engineering or equivalent technical field required


* A minimum of 7 (five) years of relevant professional work experience in the field regulated health industry : Cosmetic/Device/Drug regulated environment

• Experience in Quality systems, supplier management, labeling, GxP documentation (SOPs and specifications approval, Change control management) audits/regulatory inspections

• Proven experience in working on virtual teams within dynamic settings in a regional /cross-functional environment.

Ideally 2-3 years.


* Solid technical (quality/regulatory) knowledge


* Understanding of LATAM GxP regulations applicable for cosmetics, devices, pharmaceutical industries.

Desired Qualifications /Technical com...