Especialista en Garantia de la Calidad

Especialista en Garantia de la Calidad

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:

COORD QA

Location:

Latin America, Mexico, Distrito Federal, Mexico City

Work Location:

Hybrid

What you will do

The Quality Assurance Specialist will be part of the LatAm Source Quality organization and is responsible for maintaining quality records, coordinating change control processes, and supporting corrective and preventive actions. You will analyze data, assist in external suppliers’ audits, and help improve external manufacturing processes to ensure compliance and enhance quality:

Key Responsibilities

• Act as Quality key driver in multiarea projects.
• Lead cross-functional teams in developing and executing continuous improvement initiatives, resolve quality issues, and support technology transfer activities.
• Collaborate with R&D and production units to embed Quality assurance principles early in the development process, ensuring compliance, efficiency, and readiness for audits and inspections.
• Design and implement advanced Quality assurance frameworks that proactively identify and mitigate risks throughout the product lifecycle.
• Develop, propose, and assist in implementing corrective and preventive action (CAPA) plans, monitor their effectiveness, and ensure timely closure while maintaining accurate and timely quality records related to product testing, nonconformance, project outcomes, and stakeholder feedback.
• Foster a culture of excellence, and assist in the development, implementation, and periodic review of standard operating procedures, especially for interactions with external manufacturers and suppliers.
• Coordinate and manage change control documentation and approval processes to ensure compliance and traceability, assess current quality systems, recommend and implement improvements to enhance quality and reduce cycle times, and monitor quality trends to proactively identify and address issues.
• Guarantee projects’ compliance, accuracy, and alignment with company policies, procedures and global/local quality standards.

 

What we are looking for

Required Qualifications

• Bachelor’s degree or equivalent in Engineering, Quality Management, or a related field.
• 6 to 8 years of progressive experience in quality assurance roles within regulated industries.
• Knowledge in Drug Product Manufacturing and Controls.
• Strong knowledge on regulatory requirements across LatAm region such as ANVISA, COFEPRIS, INVIMA, ANMAT.
• Strong knowledge of quality management systems, and process criteria.
• Proven experience in managing CAPA processes and conducting root cause analysis.
• Demonstrated ability to coordinate audits and inspections successfully.
• Excellent analytical skills with the ability to interpret data and generate actionable insights.
• Effective communication and coordination skills to work with cross-functional teams and external stakeholders.
• Ability to develop and implement quality improvement initiatives and standard operating procedures.
• Proven experience supporting technology transfer activities, process validation, and manufacturing process improvements.
• Advanced to Fluent English.

Desired Qualifications

• Basic to Intermediate Portuguese.
• Influence stakeholders at all organizational levels.
• Proven ability to lead multidisciplinary teams and drive quality initiatives that result in measurable improvements in product performance.
• Proficiency in leveraging data analytics tools to enhance decision-making and predictive quality measures.
• Exceptional problem-solving skills combined with a visionary approach to quality challenges, enabling the anticipation and resolution of complex issues.
• Demonstrated expertise in innovative quality control techniques and process optimization.
• Advanced technical training and experience using Statistics, Lean and Six Sigma Methodologies.

 

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