- Type of professional relationship: Contract
- Type of contract: Indefinite
- No. Weekly hours: 38
- Hours: 8:30/9:30 a.m. to 5:00 p.m./6:00 p.m. (includes weekends when needed)
- Gross annual salary: 24720
- Professional category: Senior and similar technicians
- Regular training required: e. Superior CFG - e. CFG Superior, e. Superior CFG - e. Superior CFG
- Complementary training: - Background experience in Quality Systems.
- Experience in a biomedical laboratory.
- High level professional training (FP2), intermediate level training cycles, baccalaureate, or an equivalent qualification. - Computer skills: Microsoft office
- Other specific requirements: -Availability to work during weekends.
-Experience in Quality Control procedures.
-Experience in cell culture and molecular biology.
- Knowledge of Good Manufacturing Practices (GMP).
-Knowledge of UNE-EN ISO 9000. - Most developed personal skills: Teamwork and Cooperation, Learning and use of knowledge, Flexibility and Change Management, Commitment to the Organization, Planning and organization, Initiative, Concern for order and quality
- Languages: English - Advanced, Spanish - Advanced, Catalan - Advanced
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40669 - Quality Control technician - Barcelona, España - Barcelona Activa
Descripción
The Quality Control Technician position is available in a Production and Validation Center of Advanced Therapies. The position involves the tasks of the technician for the Quality Control of production of Advanced Therapy Medicinal Products (ATMPs) for all medical disciplines.
The Area for Clinical Production is involved in the following processes:
-Cell-based therapeutic products.
-Gene therapy products and lentiviral production in our GMP facility.
-Tissue engineering products and production of artificial scaffolds.
-3D bioprinting tissues.
-GMP and UNE-EN-ISO:9001 protocols.
This work will be performed at the Clinical Area in close contact with the laboratory of Stem Cell and Regenerative Medicine. The center is integrated in the Spanish network of Advance Therapies (RICORDS; TERAV), which provides a collaborative environment to successfully achieve our objectives.
Main Duties
- Perform quality control tests for clinical productions and facilities
- Management of reagents, materials and equipment
- Support in production processes.