Ofertas de empleo para Aptitudes de laboratorio

• Nivel de experiencia---
• Tipo de contratoA tiempo parcial
• Publicada3 mar.

Inglés Ingeniería Control de calidad Manufactura Análisis de causa raíz Resolución de incidencias Sistemas de calidad Aptitudes de laboratorio Análisis de peligros y puntos de control críticos 5S

Descripción del empleo:

Empresa dedicada a la fabricación y venta de productos de panadería y pastelería busca incorporar a su equipo un tecnico/a de calidad.

Principales funciones:

- Control de seguridad alimentaria y normativa

- Elaboración de informes alimentarios

- Control de procesos y producto

- Gestión de la trazabilidad

- Implementación y seguimiento del sistema APPCC ( Análisis de peligros y puntos de control críticos)

Se requiere:

- Formación: Técnico superior en procesos y calidad en la industria alimentaria/ Ciencia y tecnología de los alimentos y/o similar

- Experiencia 2 o mas años en calidad

- Conocimientos actualizados de normativa alimentaria

- Manejo fluido de herramientas ofimáticas

- Capacidad para trabajar en equipo

Se ofrece:

- Jornada parcial

- Estabilidad laboral

- Proyecto de desarrollo profesional

- Entorno de trabajo familiar y colaborativo

Tipo de puesto: Contrato indefinido

Experiencia:

• Control de calidad: 2 años (Deseable)

Ubicación del trabajo: Empleo presencial

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada24 feb.

Inglés Excel Español Física Capacidad de análisis Google Cloud Aptitudes de laboratorio Cultivos celulares PCR en tiempo real Principios de Préstamos Verdes (GLP) Word

MAIN DUTIES & RESPONSIBILITIES

• Prepare analytical batches to quantify drugs, anti-drugs antibodies or biomarkers in biological matrices by ligand binding assays (ELISA, MSD) according to international guidelines and internal procedures.
• Perform the evaluation and treatment of results of analytical batches.
• Label proteins with biotin or Sulfo-tag.
• Support the Study Director in: (i) the resolution of problems, (ii) the preparation of SOPs and other study documentation.
• Carry out maintenance and calibration/verification of laboratory equipment.
• Actively support Laboratory Management in evaluating and implementing new processes and equipment.

REQUIRED PROFILE & QUALIFICATIONS

• PhD, MSc or BSc in biology or related subject.
• Minimum 1-year experience in bioanalytical laboratories.
• Experience working with ELISA, MSD or other Ligand Binding techniques.  
• Understanding of international bioanalytical guidelines, and experience working under GLP/GCP regulations.
• Experience working with LIMS systems and with cell culture and qPCR techniques will be valued.
• Excellent level of English (Spanish – nice to have).
• Proficiency in MS-Office, especially Word and Excel.

OTHER REQUIRED SKILLS

• Strong communications and organization skills, and capacity to work in teams.
• Proactive and hands-on approach.
• High level of motivation and enthusiastic personality.

WHAT IS OFFERED

• Opportunity to work and contribute to the success of an expanding CRO.
• Solid scientific team with career growth opportunities.
• Cutting edge laboratory with the latest technology.
• International and multicultural environment in company based in Barcelona.
• Diligent, professional organization, with a human touch.

COMPANY DESCRIPTION

Anapharm Bioanalytics is a customer-driven Contract Research Organization (CRO) specializing in small and large molecule bioanalysis. With over 30 years of expertise in method development, validation, and sample analysis, the company supports drug development for pharmaceutical and biotechnology industries globally. Anapharm leverages advanced LC-MS/MS and LBA technologies to deliver services such as PK studies, biomarker testing, and immunogenicity assays for preclinical and clinical phases. The organization maintains strict compliance with GLP and GCP standards, having successfully passed multiple regulatory inspections by authorities such as the FDA and EU Health Authorities. Through a global network of partners, Anapharm offers robust full-service solutions for drug development and regulatory approval.