Full-Time Analista Control de Calidad Bio
Descripción del empleo
Overview:
Perform operations related to product stability following the operating procedures of your area and the requirements of GMP regulations, in order to perform biochemical stability analyses.
Responsibilities:
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• Biochemical control of samples during stability:o Prepare materials and set up equipment.o Prepare, control, and manage the reagents and solutions required for the tests to be performed.o Perform maintenance on the equipment and materials required for these analyses in the laboratory.o Perform biochemical analyses of samples:o ELISA (potency)o SDS-PAGEo Bioassayso Cell culture maintenance• Conduct the training required to perform their duties and provide training to other analysts as appropriate.• Initiate investigations into discrepancies, incidents, or out-of-specification results, following the established system at the plant.• Reception of the material used in the QC laboratories.• Correct documentation of all process-related activities, always complying with operating procedures and GMP regulations.o Document all activities performed during the testing/inspection process.o Execute the required activities in the laboratory management system (LIMS)o Prepare, review, and propose modifications to SOPs, EPRs, PTs, and Training Guides.
Qualifications:
Education: Professional training in science or higher• Languages: Fluent in Spanish and intermediate in English• Experience (years/area): > 1 year in the pharmaceutical/biotechnology industry or laboratory experience• Specific knowledge: Biochemical techniques: SDS, ELISA, bioassay, cell culture• Travel: N/A• Personal skills: Organized, teamwork, ability to organize tasks, and proactivity.
58 Visitas totales, 1 Hoy