Toxicologist - 92816

☞ AUSY by Randstad

Ver: 115

Día de actualización: 26-11-2025

Ubicación: Wavre Walloon Brabant

Categoría: Gerencia ejecutiva Producción / Operación

Industria:

Tipo de empleo: Voltijds

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Interested ? Don’t hesitate to take a look at the job description below and contact me !


  • Master’s degree or PhD in pharmacy / toxicology or related areas
  • At least 3 years full-time experience in a pharma company, working in quality, drug, safety or regulatory affairs or other where evaluations related to patient safety were part of the activities performed
  • Knowledge of GMP regulations
  • Good understanding of PV practices
  • Demonstrated ability to think critically and innovatively, identify and solve problems
  • Influencing / persuasion skills
  • Proven ability to interact well in a multi functional team setting
  • Commitment to continuous improvement
  • Excellent communication skills
  • Fluent written and spoken English


Consultancy


We offer an attractive salary with extra-legal advantages:

  • Group insurance
  • Hospitalisation insurance
  • Meal vouchers of 7 euros gross per working day
  • Reimbursement km or company car
  • Monthly allowance (80 euros net per month)
  • A 13th month
  • Training
  • Etc.

A rate is freelance is also possible


Our client is a global vaccine research, development and production company, that employs over 11,200 people worldwide, of which 7,500 in its three Belgian sites: Rixensart, Wavre and Gembloux.


Job purpose:


To provide toxicological expertise and support for global manufacturing and global quality for all matters related to quality issues in manufacturing (e.g. residuals, contaminants, E&L, raw mats, PIRCs, intelligence re: vaccine / adjuvant quality standards and regulations). The integration of this function into safety enables direct risk assessment for patient safety.

Key responsibilities:


  • Performing toxicological risk assessment s and delivering toxicological analyses reports
  • Conducting literature searches for nonclinical toxicology and safety information
  • Maintaining a toxicological database for residuals and contaminants
  • Following up on inquiries from GIO and global QA (for example provision of expert toxicological advice for deviations, extractables and leachables and other manufacturing quality issues)
  • Complementing the toxicological investigations by clinical safety assessments when applicable
  • Interacting with GIO, GQ, GRA and other safety groups to acquire expertise necessary to perform the job and to facilitate integrated assessments
  • Providing support to the team in their routine and ad-hoc activities such as data management and signal detection and evaluation)
  • Improve process for the patient safety toxicology risk assessment of GMP
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Plazo: 10-01-2026

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