Senior Project Toxicologist (all genders)

Posted 28 Mar 2024

Darmstadt, Hessen - Germany

Req Id 273451

 

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

 


Senior Project Toxicologist

We are seeking a highly motivated and team-oriented Senior Toxicologist to join our Nonclinical Safety Global Project Strategy and Science (PSS) team in Ivrea, Italy, or Darmstadt, Germany. In your role, your primary responsibility will be to plan and oversee nonclinical safety programs to support the development of drug candidates from discovery to market authorization.

Your role

You will develop and implement safety strategies for a portfolio of projects in various indications with a focus on new modalities, but also including small and large molecules and ADC’s. You will serve as the main interface between Global Program Teams and Nonclinical Safety Global Project Strategy and Science (PSS), ensuring alignment and effective communication. You will analyze toxicology and safety pharmacology data and collaborate with cross-functional teams to ensure effective implementation of safety strategies. You will author nonclinical safety sections of various regulatory documents. You will provide expertise in due diligence reviews and offer recommendations for partnerships or in-licensing opportunities.

Who you are

  • Advanced scientific degree (DVM; PhD in life sciences, Toxicology, Biology, Physiology).
  • Certification in Toxicology by Toxicology Board or certification in Pharmacology and Toxicology is desirable.
  • Minimum of 7 years' experience in a pharmaceutical project environment with a strong understanding of drug development and discovery processes and workflows.
  • Broad knowledge in the field of toxicology and safety pharmacology.
  • Solid expertise in the field of ADC’s or new modalities such as targeted protein degraders is a plus.
  • Solid understanding of regulatory guidelines and experience preparing submission documentation. Familiarity with health authority interactions and MAA submissions is advantageous.
  • Strong ability to work effectively in a team environment and demonstrate inter-cultural understanding.
  • Excellent communication skills, both oral and written, in an interdisciplinary environment.
  • Strong organizational skills and proficiency in spoken and written English.

Location: The position will be based in Ivrea, Italy or Darmstadt, Germany.



What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 
Apply now and become a part of our diverse team!


US Equal Employment Opportunities

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law.  This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

We are committed to an equitable hiring process for candidates from a diverse range of backgrounds. As part of this commitment, applicants with disabilities may be entitled to reasonable accommodations. Please contact USLeavesandAccommodations@milliporesigma.com, if a reasonable accommodation is needed or if you otherwise need assistance to participate in the hiring process.


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