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Parenteral Support Operator I

Barceloneta, PR Temporero Publicado 12 oct 2026
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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.

Lo que piden, en corto
  • 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 26 días. Kelly Services tiene 137 plazas abiertas más en MyPRjobs. En Barceloneta hay 70 empleos activos más.

Resumen

At Kelly® Science, Engineering, Technology & Telecom (SETT) , we’re passionate about helping you find a job that works for you. How about this one?

We’re seeking an Parenteral Support Operator I to work with one of our top global biopharmaceutical clients in the Barceloneta PR area.

Operate different equipment in one of the functional areas assigned. Perform inspection and pack syringes. Assemble and inspect equipment in the manufacturing area to confirm operational status. Perform cleaning and sterilization procedures. Work is performed in aseptic or non-aseptic environments.

Responsibilities:

•Inspect and pack syringes of biologic parenteral product.

•Clean, prepare and sterilize manufacturing equipment for parenteral use.

•Conduct equipment and facility inspections and raise situations that affect the operating, safety, and environmental conditions.

•Receive, inspect and verify materials availability to be used for production. Sample collection and processing as required by the process.

•Document, audit documentation and timely correct manufacturing electronic or paper batch record discrepancies.

•Perform cleaning operations according to the established procedures.

•Document process and equipment status in the area electronic or manual records.

•Monitor critical parameters and raise any deviation that could impact the operations to address accordingly.

•Strict adherence to current Good Manufacturing Practices (cGMP’s), Standard Operating Procedures (SOP) and accurately complete process-associated documentation.

Qualifications:

•Degree in Science, Mechanics, Electricity, Instrumentation or related field.

•No previous experience required

•Basic knowledge of laboratory techniques.

•Basic knowledge of computerized systems such as Delta V, MES and SAP preferred.

•Basic mechanical and mathematical skills.

•Basic verbal and written communication skills in English and Spanish.

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