Privado

Senior QA Auditor

Kelly Services

Juncos, PR $48 / hora Temporero Publicado 24 sept 2026

Solicitar empleo

Prepárate para solicitar (2 min)

MyPRjobs no procesa esta solicitud. Serás dirigido al portal oficial del patrono.

Crear résumé para este empleo

Lo que debes saber de esta plaza

Preparado por MyPRjobs con los datos del anuncio y de nuestro catálogo. El anuncio del patrono sigue más abajo, completo.

Este tipo de trabajo

Trabajo en plantas de manufactura, farmacéuticas o de equipos médicos. Se opera maquinaria, se ensambla, se empaca o se inspecciona calidad siguiendo procedimientos estrictos (GMP). Muchas plantas trabajan por turnos rotativos.

Cómo está el pago

Anuncia $48.00 por hora. Es 26% más que la mediana de plazas parecidas en Juncos ($38.00, de 15 anuncios). Está por encima del salario mínimo de Puerto Rico ($10.50).

Lo que te quedaría a la semana (aproximado)

A 40 horas: $1,920 brutos y unos $1,767 después de Seguro Social (6.2%), Medicare (1.45%) y SINOT (0.3%).

Antes de la retención de contribución de Hacienda, que depende de tus exenciones (formulario 499 R-4), y de plan médico o retiro si te los descuentan.

Lo que piden, en corto

Bachillerato
Inglés o bilingüe

Documentos que suelen pedir

Identificación con foto y Seguro Social o permiso de trabajo (formulario I-9)
Diploma de cuarto año
Certificado de buena conducta (antecedentes penales), en algunas plantas

En nuestro catálogo

Publicada hace 45 días. Kelly Services tiene 136 plazas abiertas más en MyPRjobs. En Juncos hay 166 empleos activos más.

Más de Kelly Services

Todos los empleos en Juncos →Crea tu résumé sin costo →

Resumen

At Kelly ® Science, we’re passionate about helping you find a job that works for you.

We’re seeking Senior QA Auditor to work for one of our top biotechnology industry clients at Juncos, PR .

Salary: $48.00 hr

Shift: 8hrs shift | Administrative – with work schedule flexibility as required to support 24/7 operations, requiring occasional after-hours engineering coverage.

Why you should apply to be Senior QA Auditor:

- Competitive pay rate and opportunity for professional growth

- Work with a leading organization in the manufacturing sector

- Engage in diverse, impactful engineering projects

- Contribute to a culture of safety, innovation, and operational excellence

- Bi-Weekly pay by W-2

- Vacations, Sick & Holidays paid*

- Christmas bonus *

*Must comply with minimum established requirements to qualify.

This job might be an outstanding fit if you have the following qualifications:

- Doctorate with 2+ years, Master’s with 4+ years, or Bachelor’s with 6+ years of directly related Quality Assurance, Validation, or Manufacturing experience. ( Degrees in Life Science or Engineering)

- Strong knowledge of GMP regulations, Good Documentation Practices, Data Integrity, Quality Systems, Change Control, Risk Management, and validation lifecycle activities.

- Experience auditing and supporting manufacturing processes, process validation, equipment qualification, facilities/utilities commissioning and qualification, and Computer System Validation (CSV).

- Demonstrated ability to lead audit investigations , assess compliance issues, perform risk assessments, and drive effective corrective and preventive actions (CAPAs).

- Experience working with quality and manufacturing systems including KNEAT, CDOCS, SCADA, TrackWise, Maximo, or similar platforms.

- Strong technical documentation, written and verbal communication skills (English & Spanish)

The Senior QA Auditor serves as the Quality Assurance technical lead, providing oversight and approval of manufacturing processes, validation activities, investigations, and quality systems. Partner with cross-functional teams to ensure GMP compliance, support new product introductions, manage quality risks, and drive continuous improvement across manufacturing operations. Designs, monitors or conduct experimental strategies. Provides data analysis and interpretation and assesses impact of the data on the project. Review and approve manufacturing processes, validation protocols and reports, environmental characterization reports, planned incidents, and sanitary utility system releases while ensuring compliance with GMP requirements. Lead quality audit investigations, represent QA on cross-functional teams and governance boards, support new product introductions, and maintain site quality programs and procedures.

Helping you discover what’s next in your career is what we’re all about, so let’s get to work.

Apply to be a Senior QA Auditor today!

Lilly Abouomar 9395454792

#Kelly80 #SETTPuertoRico #QA #biotechnology