Regulatory Toxicologist for Medical Devices (m/f/d)

in permanent employment

Whether for the registration of agrochemicals, biocides, veterinary pharmaceuticals or medical devices - as a leading service provider in consulting for the chemical and pharmaceutical industries, our client has been setting global quality standards for many years, with more than 550 employees. Based on more than twenty years of experience and constant focus on optimization, our clients' experts have a deep understanding of customers' products and can provide the best possible solution for each customer.


To support our clients' team we are currently seeking a

Regulatory Toxicologist for Medical Devices (m/f/d)

in permanent employment

  • Bereich:


  • Berufssparte:

    Zulassung/Regulatory Affairs

  • Arbeitsregion:

    Mannheim area / Leverkusen area

  • Art der Anstellung:


  • Kennziffer:


  • Aktualisierung:


Have we aroused your interest?

Then apply online or by e-mail right here, stating your earliest possible starting date and your desired salary.

Your tasks

  • Toxicological / biological evaluation of medical devices in the framework of the Medical Device Regulation (MDR), ISO 10993-series and other relevant regulatory guidelines/requirements
  • Development of biological evaluation strategies
  • Searching for relevant literature and evaluation of toxicological studies and publications for critical human health effects
  • Performance of toxicological risk assessments for medical devices, based on the used raw materials, on extractable and leachable chemicals or on biocompatibility studies
  • Preparation of scientific expert statements
  • Assurance of high quality within projects (i.e. reports, expert statements)
  • Communication and close co-operation with customers

Your qualification

  • University degree preferably in toxicology, biology or a related field
  • DGPT courses in toxicology or equivalent toxicological qualifications would be an asset
  • Experience in medical device toxicology would be an asset
  • Knowledge of risk assessment process and of in vivo and in vitro methods for safety / toxicology assessment would be an asset
  • Excellent language skills in English and German (spoken and written); additional language skills would be an asset
  • You have a strong motivation and ability to communicate in a multinational environment
  • You are able to work in a team as well as self-motivated
  • You have a service oriented personality and attitude
  • You are a quick learner and able to react to new challenges

We offer

  • You will work in a dynamic field in a collegial and appreciative team
  • A well-structured induction plan will make your start easier and your further education will be supported by our clients Academy
  • On average each employee has 3 days of further education per year
  • We support you in balancing your work and private life and offer you 30 days of vacation, a childcare allowance and family-friendly flexible working time models
  • In addition to your fixed salary, we grant your commitment with performance-related bonuses
  • We provide you with a lucrative employee participation program
  • You will receive a canteen allowance and we will offer you coffee, tea and water for free
  • To strengthen our team spirit, team events are held in addition to the annual employee meeting
  • We also ensure your financial stability after retirement - through the offer of a company pension plan

Ihre Ansprechpartnerin

Bettina Cöppicus
Senior Personalberaterin


Optares ICM GmbH & Co. KG
Bettina Cöppicus
Heiligengeist Höfe 8
26121 Oldenburg