Toxicologist (Pharma Industry)

Hiring By - Biostaffic

 BioPharma

Community of Madrid - Spain

Job Highlights

Not Disclosed

Posted 4 months ago
Job details

#WeareAzierta, part of the #QbDGroup, a pharmaceutical consulting firm, partner of life sciences companies. We globally support our clients in the development, transformation and integral management of the life cycle of their products and services, resulting in a premium service of high quality consulting, always for the benefit of patients and consumers worldwide.


We are looking for a Toxicology Profile with at least 1 year of experience in industrial toxicology and/or ecotoxicology and environmental risk assessment, as well as knowledge of regulation and GMP regulations.


If you want to know more about the job... keep going!



What kind of profile are we looking for?


  • Bachelor's degree in Toxicology, Chemistry, Pharmacy or other related field or university degree in Environmental Sciences, Ecology, Biology or related discipline.
  • Knowledge of REACH, IUCLID and CLP regulations.
  • Experience in the preparation of technical documents
  • Experience in industrial toxicology, preferably in the assessment of extractables and leachables and/or environmental and ecotoxicology.
  • Experience in the establishment of PDE (Permissible Daily Exposure Limit) and OEL (Occupational Exposure Limit) values.
  • Knowledge of the rules and regulations in industrial toxicology.
  • Experience in analytical techniques.



What will be your key responsibilities?


  • Evaluation of Extractables and Leachables:

Perform detailed analysis of materials and products to identify impurities in extractables and leachables. Risk assessment and toxicological evaluation of detected impurities.

  • Establishment of PDE and OEL:

Determine the Permissible Daily Exposure Limits (PDE) for chemical substances in products and processes.

Define Occupational Exposure Limits (OEL) to protect workers' health.

  • Regulatory Compliance: Keeping up to date on regulations and standards related to industrial toxicology.
  • Environmental Risk Assessment:

Conduct environmental risk assessment reports to evaluate the impact of chemicals on aquatic and terrestrial ecosystems. Identify and quantify the environmental risks associated with the use of chemical substances.

Apply in-depth knowledge in the implementation and enforcement of REACH requirements.

Experience in preparing dossiers using IUCLID for the registration of chemicals.

Interpret and apply classifications and labelling according to the CLP Regulation.



What is waiting for you?


  • A company with a clear strategy and ambition where the people centric approach and business go hand in hand. You will be part of the ever-growing #QbDCompany! What does it means?


  1. We offer sustainable careers and meaningful connections.
  2. We are a knowledge based company.
  3. You’ll work for an award winning company: Best Managed Company (Deloitte award).


  • 3Fs: Fast pace of work, fast learning, fast growth.
  • Full-time work with the opportunity of a hybrid work format.
  • Salary package adapted to your experience.



If you are interested in joining a challenging project, have initiative, the ability to work in a results-oriented, fast-paced work environment, and have explosive growth prospects... this is your place. Go fast, send us your CV!

Benefits Offered?

  • No

Bonus Offered?

  • No

Travel Required?

  • No

Location:

  • Community of Madrid - Spain

Global Experience Needed?

  • No

Specialized Experience Needed?

  • No

Apply before:

  • Apr 14, 2024
Company Overview
Azierta | Part Of QbD Group
Azierta | Part Of QbD Group

Current Openings: 0

Azierta es consultora especializada en Ciencia y Salud que apuesta por potenciar las relaciones entre la ciencia y el entorno empresarial a través del concepto “Science to Business to People”. Prestamos servicios en el ámbito de medicamentos, productos sanitarios, cosmética, higiene, complementos alimenticios y biocidas, ofreciendo soluciones globales en todo el ciclo de vida de los productos, desde el soporte médico y regulatorio, hasta las necesidades a nivel de toxicología, fabricación y distribución, acceso al mercado y farmacovigilancia. Hemos colaborado con más de 300 clientes en el entorno europeo a través de un equipo experto multidisciplinar, siempre orientados a la obtención de resultados y teniendo muy presentes las necesidades de nuestros clientes.
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