Pharmaceutical Mixing Technician III

Quality Consulting Group, LLC tiene disponible una oportunidad de empleo para Pharmaceutical Mixing Technician III.

La ubicación informada para la plaza es Jayuya.

La información de la vacante indica lo siguiente: quality Consulting Group is seeking a Pharmaceutical Mixing Technician III to support manufacturing operations in Jayuya, Puerto Rico. This position is responsible for weighing, preparing, and mixing pharmaceutical raw materials while operating and monitoring specialized production equipment in accordance with established manufacturing, quality, and safety procedures.

The technician will prepare pharmaceutical mixtures using raw materials such as amino acids, Metronidazole, Heparin, Milrinone, and other compounds; operate mixing equipment, valves, and auxiliary systems; perform material weighing and sampling activities; and maintain accurate production documentation.

The role also involves monitoring equipment performance, troubleshooting routine manufacturing and material issues, supporting validation and new-product activities, conducting inventory counts and area inspections, and ensuring that the mixing area remains clean, organized, and inspection-ready.

La publicación señala los siguientes requisitos: All work must be performed in compliance with SOPs, cGMPs, cGDPs, CFR requirements, safety regulations, and Good Documentation Practices. Candidates should have an Associate's Degree, with a Bachelor's Degree preferred, along with previous experience in pharmaceutical, medical device, manufacturing, sterilization, or mechanical equipment operations. The position requires strong attention to detail, basic mechanical troubleshooting skills, the ability to work independently and as part of a team, and the physical ability to manually handle materials weighing up to 100 lbs. Candidates must also be available to work flexible schedules, including weekends and overtime, based on production requirements.

Fuente: qualityconsultinggroup.applytojob.com

All work must be performed in compliance with SOPs, cGMPs, cGDPs, CFR requirements, safety regulations, and Good Documentation Practices.Candidates should have an Associate's Degree, with a Bachelor's Degree preferred, along with previous experience in pharmaceutical, medical device, manufacturing, sterilization, or mechanical equipment operations. The position requires strong attention to detail, basic mechanical troubleshooting skills, the ability to work independently and as part of a team, and the physical ability to manually handle materials weighing up to 100 lbs.Candidates must also be available to work flexible schedules, including weekends and overtime, based on production requirements.