Analista de Calidad – Industria Farmacéutica

SGS • Spanish: C1 • Biotechnology • Science & Engineering • 3 months ago
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Salary
≈ $26k – $68k per year (Estimated)
Location
Remote/Hybrid (Buenos Aires, Argentina)
Seniority
Intern
Employment
Full-Time
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SGS

SGS is a Swiss testing, inspection and certification company founded in 1878 as a grain inspection house in Rouen and now one of the largest verification businesses in the world. It tests and certifies goods, systems and facilities across agriculture, minerals, oil and gas, chemicals, consumer products, industrial equipment, transport and life sciences, acting as an independent third party between buyers, sellers and regulators. Headquartered in Geneva and listed on the Swiss exchange, it operates thousands of laboratories and offices and employs around one hundred thousand people worldwide.
sgs.com • HQ: Geneva, Switzerland • Cybersecurity • Biotechnology • Testing, Inspection & Certification • Environmental Science • Science & Engineering • Professional Services • 5000+ employees • Est. 1878

SGS es líder mundial en inspección, verificación, análisis y certificación. Está considerada como principal referente mundial en calidad e integridad, contamos con más de 93.000 empleados y con una red de más de 2.600 oficinas y laboratorios por todo el mundo.

Brindar soporte al área de Calidad, asegurando el cumplimiento de las Buenas Prácticas de Manufactura (GMP), procedimientos internos y requisitos regulatorios aplicables, contribuyendo al mantenimiento y mejora del Sistema de Gestión de Calidad.

  • Ejecutar actividades de control y aseguramiento de la calidad conforme a procedimientos establecidos.
  • Elaborar, revisar y controlar documentación del Sistema de Gestión de Calidad (POE, registros, instructivos y especificaciones).
  • Participar en la gestión de desvíos, investigaciones y controles de cambios.
  • Colaborar en auditorías internas y brindar soporte durante inspecciones de organismos regulatorios.
  • Realizar seguimiento de acciones correctivas y preventivas.
  • Participar en actividades de validación y calificación cuando sea requerido.
  • Colaborar en programas de capacitación relacionados con Calidad y GMP.
  • Gestionar indicadores del área y elaborar reportes.
  • Promover la mejora continua y el cumplimiento de las normas de calidad y seguridad.

  • Valor agregado (deseable)

  • Conocimientos en normas ISO 9001 - 17025 - GMP
  • Manejo de herramientas de gestión (checklists digitales, reportes)
  • Interés en desarrollo en entornos industriales / laboratorio
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