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In compliance with Organic Law 15/1999, of 13 December, under the Personal Data Protection Act, we inform you that data collected will form part of an automated file, under the ownership of BARCELONA ACTIVE SPM S.A., with registered office at 162-164 Calle Llacuna, Barcelona, with the aim of managing enrollments and of informing of the company's activities and services within its field of action. You will be able to exercise access rights, rectification, cancel cancellation and/or opposition via written communication to the Legal Services of BARCELONA ACTIVE SPM S.A. at the aforementioned address.

 
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Description

Toxicology can be defined as the discipline which studies the harmful effects of chemical and physical agents (toxic agents) on biological systems, and one which also establishes the extent of the damage caused by the exposure of living organisms to these agents. The professional toxicologist studies the safety of drugs, foodstuffs and other substances. The work of a toxicologist consists of planning, directing and interpreting laboratory and field studies and to identify and assess the toxic effects of a broad range of substances and materials, such as, for example, the safety of new chemicals destined to pharmaceutical use, agricultural products, groceries and other consumer products. The professional toxicologist operates in an environment which includes biopharmaceutical laboratories, technical-scientific services and public safety institutions, analysing potential toxic effects, whether in-vitro (in cell cultures) or in-vivo (in animals).

Tasks

  • Plan and carry out safety experiments required by law and agencies (Spanish Medication Agency, European Medicines Agency and the US Food and Drug Administration) to authorise the registration and commercialisation of drugs, animal health products and some cosmetic and nutrition products (functional foods).
  • Design and carry out preclinical trials involving animals or in vitro systems, using bacterial, cell or tissue cultures. Also involved in clinical trial sample analysis.
  • Carry out histopathological analyses of biological samples and maintain contact with laboratories and analysis technicians to obtain additional results.
  • Gather statistical data regarding the assessment and carry out an analysis of potential risks, subsequently issuing the relevant advisory reports.
  • Operate under quality assurance and control regulations GLP and GCP (Good Laboratory and Clinical Practice, respectively) in the case of laboratory biopharmacists, and under ISO regulations in the case of environmental matters or other.
  • Lead and coordinate a team of laboratory assistants, supervising the fulfillment of regulations and data collection.
  • Maintain permanent contact with those in charge of quality and regulatory matters to ensure adherence to regulations and experiment design, as well as with physicians and clinical staff in order to gain an in-depth knowledge of pathologies and know how to extrapolate symptoms and test conclusions.
  • Publish articles in specialised journals and attend specific conferences.

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Centre per al desenvolupament professional Porta22
Convent de Sant Agustí
Ca n'Andalet

Barcelona Treball (Porta22)
+34 934 019 899
bcn.cat/treball

Barcelona Activa Headquarters
Llacuna, 162-164
08018 Barcelona
+34 934 019 777
bcn.cat/barcelonactiva

Generalitat de Catalunya
Unió Europea FEDER
Unió Europea FSE