Project Toxicologist (m/f/d)

Our mandator is the global leader in the pharmaceutical Biotech Industry and develops innovative and best in class agents in the area of Oncology/Hematology, Immunology, Nephrology, Oesteoporosis and many more.


For the Department of Comparative Biology and Safety Sciences we are searching as soon as possible for a dedicated and highly motivated

Project Toxicologist (m/f/d)

  • Bereich:

    Medical

  • Berufssparte:

    Produktions-/Fertigungsmanagement

  • Arbeitsregion:

    Greater Munich area

  • Art der Anstellung:

    Permanent

  • Kennziffer:

    24630

  • Aktualisierung:

    03.12.2018

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Your Responsibilities

  • Developing in-depth understanding of and strategies for characterising and managing target liabilities
  • Developing and implementing toxicology strategys for early through lead optimization and candidate selection
  • Designing and implementing exploratory and regulatory toxicology studies
  • Managing and analying a wide range of literature and datasets
  • Working cross-functionally to contribute to program development by acting as a representative for the company's Area
  • Liaise within the Area of the company to leverage internal subject matter expertise in pre-/non-clinical safety assessment
  • Participate in activities related to the application (CTA/IND) and market authorization
  • Working in multi-disciplinary international teams

Your Qualification

  • Degree with at least three years of relevant scientific experience (Doctorate/Veterinary or PhD) including toxicology (ideally a certification or master’s degree)
  • Experience in the post-doctoral research in the discipline of interest/relevance (e.g. molecular/cellular biology, immunology, oncology or pathology)
  • Experience (Academic, CRO and/or industry)in pre-/non-clinical drug development demonstrating a sustained record of achievement and the ability to understand translational biology
  • Excellent communication skills (German and English)
  • Experience resolving scientific problems through the establishment of novel scientific approaches
  • Ability to critically evaluate, interpret and integrate large datasets and literature
  • Understanding of cutting-edge science and technology employed to enhance the investigation of drug candidate safety liabilities
  • Experience interacting with regulatory agencies
  • Ability to work independently, build productive cross-functional collaborations, multi-task and prioritize
  • Proven learning agility, resilience and teamwork skills
  • Interest and ability to serve as a subject matter expert in a specific discipline

Ihr Ansprechpartner

Inken Steinkamp
Personalberaterin

Anschrift

Optares Medical GmbH & Co. KG
Inken Steinkamp
Heiligengeist Höfe 8
26121 Oldenburg