ANALISTA SR DE GARANTIA DE QUALIDADE at Kenvue · São José…

Kenvue is currently recruiting for a:ANALISTA SR DE GARANTIA DE QUALIDADE

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: GERENTE DE GARANTIA DE QUALIDADE

Location: Latin America, Brazil, Sao Paulo, Sao Jose dos Campos

Work Location: Fully Onsite

What you will do

Act as a strategic quality partner overseeing validation and qualification strategies and approvals, driving cross-functional initiatives, ensuring Good Manufacturing Practices (GMP) and compliance excellence, supporting investigations and CAPA, change control impact assessment and project implementation strategies; and delivering robust quality systems, insights, and continuous improvement across complex pharmaceutical operations

Key Responsibilities • Act as Quality Partner to Qualification and Validation teams, serving as governance lead and focal point for internal action plans, validation strategies, and cross functional quality projects. • Serve as Quality partner for commissioning, qualification, and validation of facilities, utilities, and equipment, ensuring lifecycle compliance. • Review and approve cleaning validation and process validation strategies, protocols, and final reports, ensuring compliance with regulatory and internal quality requirements. • Drive cross-functional collaboration and initiatives to ensure adherence to company policies, quality standards and regulation, and ensure continuous GMP compliance and improvement • Develop, author, review, and maintain comprehensive quality system documentation including operating procedures, local procedures, and specifications within the document control system to support quality system enhancements and regulatory compliance. • Develop and present comprehensive quality performance reports to senior management, highlighting trends, insights, and strategic recommendations. • Serve as quality partner supporting site investigation, leading problem-solving and troubleshooting as well as corrective and preventive action plan (CAPA). • Support Change Control impact assessment and implementation strategy definition in partnership with the peers.

What we are looking for Required Qualifications • Bachelor’s degree or equivalent in Engineering, Science, or a related field. Pharmacy is preferred. • Strong knowledge of quality and GMP standards and regulations applicable to the pharmaceutical and or cosmetics industry. • Proven expertise in process and cleaning validation, facilities and utilities qualification. • Ability to lead cross-functional teams and communicate effectively with management and stakeholders.

• Proficiency in understanding and communicating in English

Desired Qualifications • Advanced problem-solving skills with experience in database management and quality data analysis. • Excellent technical writing skills for developing and updating operating procedures, and investigations. • Strong communication and leadership capabilities to influence cross-departmental teams and foster a proactive quality culture. • Spanish is a plus.

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.

This is a full time role requiring the selected candidate to work on site Monday to Friday

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