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Biologic Operator II

Kelly Services

Barceloneta, PR Temporero Publicado 24 sept 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.
Horario que menciona: Turno de noche · Incluye fines de semana
Lo que piden, en corto: Bachillerato
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
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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 Biologic Operator II to work with one of our top global biopharmaceutical clients in the Barceloneta PR area. With us, it’s all about finding the job that’s just right

Purpose :

Manufacture of bulk biologics products. Perform cleaning and sterilization procedures. Perform process tests and participate in qualification and validation activities as required. Assemble and inspect equipment in the manufacturing area to confirm operational status. Work is performed in aseptic and non-aseptic environments.

Responsibilities :

Operate manufacturing equipment and instruments, such as tanks, autoclaves, filtration systems, washers, filter integrity testing, pH, amongst others. Conduct equipment setup (CIP, PT, SIP) operations according to the established procedures.

Manufacture of bulk biologics operations in Media & Buffer Formulation (Central Services), Inoculum or Fermentation (Upstream) and Capture or Purification (Downstream) areas according to approved and effective procedures.

Conduct equipment and facility inspections and advise of situations that affect operating and environmental conditions. Monitor critical parameters and elevate any deviation that could impact operations to address accordingly.

Provide technical assistance to manufacturing areas, specifically the troubleshooting support of equipment and process events.

Receive, inspect and verify materials availability to be used for the production activities.

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

Document process and equipment status in electronic or manual records.

Sample collection and processing as required by the process.

Qualifications :

Associate or Bachelor Degree in Science, Mechanics, Electricity, Instrumentation or related field.

Some experience required.

Experience in GMP/ manufacturing

Daily Work Schedule Expectations 3rd shift – Training on 1st or 2nd shift – must be available for any shift/weekend