Job Description

Kenvue is currently recruiting for a:


Lead Manufacturing Associate

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.

Role reports to:

Operations Manager

Location:

North America, United States, Puerto Rico, Las Piedras

Work Location:

Fully Onsite

What you will do

Resumen de la Posicion

Como Asociado Lider de Manufactura, planificara, dirigira y coordinara los planes de produccion de los diferentes departamentos de manufactura para garantizar productos seguros, consistentes y a bajo costo. Administrara las operaciones diarias, el movimiento de materiales y el uso de sistemas de apoyo (MES & SAP), asegurando el cumplimiento con las normas de seguridad, ambientales y de calidad. Este rol tambien realiza actividades practicas de manufactura como ajustes de equipos, monitoreo de procesos y limpieza.


Este puesto se considera sensitivo por razones de seguridad.

Responsabilidades Clave

Calidad y Cumplimiento

Cumplir con las Buenas Practicas de Manufactura (GMP) y Buenas Practicas de Documentacion. Respetar estrictamente los procedimientos de la compania, seguridad e integridad. Detectar, informar y corregir desviaciones de manera oportuna. Participar en entrenamientos y promover la filosofia de "hacerlo bien a la primera".

Ambiente, Salud y Seguridad (EHS)

Cumplir con el programa de EHS y la norma ISO 14001. Mantener un area de trabajo segura (uso de EPP, proteccion contra incendios, reporte de derrames e incidentes). Apoyar programas de ergonomia y reciclaje. Reportar condiciones inseguras o incidentes de inmediato.

Responsabilidades del Area

Evaluar desviaciones y escalar al supervisor o calidad. Servir de Experto en Procesos (SME) en proyectos de mejora y transferencias. Recomendar mejoras en confiabilidad de equipos, "set up" y manejo de desperdicios. Capacitar empleados en equipos complejos (compresion, inmersion en gelatina, grabado laser, etc.). Apoyar al supervisor en la ejecucion del plan diario de produccion. Desarrollar metricas de produccion, analisis de tendencias y acciones preventivas. Revisar y aprobar registros de manufactura. Impulsar la mejora continua en procesos para cumplir con objetivos de costo, calidad y servicio.

Requisitos

Educacion:

Grado Asociado (preferible en Mecanica, Electronica o Ciencias) O seis (6) anos de experiencia en industria farmaceutica regulada con diploma de escuela superior. Se requieren destrezas de liderazgo.

Experiencia:

Minimo seis (6) anos en manufactura farmaceutica.

Conocimientos y Habilidades:

Bilingue (ingles/espanol). Conocimiento en GMP, habilidades analiticas, manejo de sistemas computarizados (Excel, PowerPoint, Word). Familiaridad con EDM, ETQ, SAP, MES.

Otros Requisitos:

Disponibilidad para horas extras y llamadas de emergencia. Apoyo a otros departamentos/proyectos segun necesidades del negocio.

Ambiente y Condiciones de Trabajo

Interior de planta con temperatura controlada y areas limpias. Exposicion a polvos, solventes, ruido y equipos de alta temperatura y presion. Requiere esfuerzo fisico liviano, destrezas manuales y agudeza visual.

Position Summary

As a Manufacturing Associate Team Leader, you will plan, direct, and coordinate the production plans of the manufacturing departments to ensure consistent, safe, and cost-effective product delivery. You will manage daily operations, oversee material movement, and support systems (MES & SAP), while ensuring compliance with safety, environmental, and quality standards. This role also performs hands-on manufacturing activities, including equipment adjustments, process monitoring, and cleaning.


This is considered a safety-sensitive position.

Key Responsibilities

Quality & Compliance

Adhere to Good Manufacturing Practices (GMP) and Good Documentation Practices. Ensure strict compliance with company procedures, safety, and integrity standards. Identify, report, and correct deviations promptly. Participate in training programs and promote "right first time" practices.

Environmental, Health & Safety (EHS)

Follow ISO 14001 and company EHS program requirements. Maintain a safe work environment through use of PPE, fire protection, spill reporting, and incident response. Support ergonomic and recycling initiatives. Report unsafe conditions or incidents immediately.

Area Responsibilities

Evaluate deviations and escalate to supervisors/quality. Act as Subject Matter Expert (SME) in process improvements and product transfers. Provide recommendations on equipment reliability, set-ups, and waste management. Train employees in complex equipment operations (compression, gelatin dipping, laser engraving, etc.). Support supervisors in executing daily production plans. Develop production metrics, trend analysis, and preventive actions. Review and approve manufacturing records. Drive continuous improvement across processes to achieve cost, quality, and service objectives.

Requirements

Education:

Associate Degree (preferred in Mechanics, Electronics, or Sciences) OR six (6) years of experience in a regulated pharmaceutical industry with a high school diploma. Leadership skills required.

Experience:

Minimum of six (6) years in pharmaceutical manufacturing.

Skills & Knowledge:

Bilingual (English/Spanish). GMP knowledge, analytical skills, computer proficiency (Excel, PowerPoint, Word). Familiarity with EDM, ETQ, SAP, MES.

Other Requirements:

Available for overtime and emergency call-backs. Able to support other departments/projects as needed.

Work Environment & Conditions

Indoor manufacturing facility with controlled temperature and clean conditions. Exposure to dust, solvents, noise, high-temperature, and high-pressure equipment. Requires light physical effort, manual dexterity, and visual acuity.

What's in it for you

Annual base salary for new hires in this position ranges:


$50.957,50 - $71.940,00
This takes into account a number of factors including work location, the candidate's skills, experience, education level & other job-related factors.

Competitive Benefit Package
Paid Company Holidays, Paid Vacation, Volunteer Time & More! Learning & Development Opportunities Kenvuer Impact Networks This list could vary based on location/region
Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.
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.


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