Validation specialist

Kenvue is currently recruiting for a:
Validation 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:
GER ENG SR
Location:
Latin America, Brazil, Sao Paulo, Sao Jose dos Campos
Work Location:
Hybrid
What you will do
Reviews and approves technical reports and other sources of information to ensure that validations and procedures are consistent with current industry, regulatory requirements, and current technology. Contributes to the development, implementation and execution of quality systems in support of qualified. Ensures that validation and qualification activities are consistent with company validation policies and procedures and federal regulations. Proceeds according to the company's quality policy in all business activities with providers and customers within and outside the company. Evaluates technical problems and provides recommendations for corrective actions. Investigates deviations to determine the impact on the product quality, the cause and corrective actions to preclude further deviations of a similar nature. Represents validation function in project teams, with the objective to assure that departmental quality objectives are met. Participates in company meetings related to changes in processes, process improvements, provide suggestions, and so on. Provides coaching and training and guidance on aspects of validations and qualifications. Provides support to internal and external customers of supplier quality in the execution of procedure and policy requirements. Acts as a major contact for validation issues during regulatory and third party in. Writes, collects, organizes and communicates data to appropriate groups.
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.