Regulatory Toxicologist (all genders)

Job Description:

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.

Regulatory Toxicologist (all genders)

Are you passionate about applying toxicological science to protect patients and support regulatory compliance? As a Regulatory Toxicologist (m/f/d) at Bayer, you will provide expert guidance on nonclinical safety topics across our global portfolio of marketed products. From evaluating impurities and defining exposure limits to developing testing strategies and supporting regulatory interactions, you will contribute to ensuring the highest standards of quality, safety and scientific excellence worldwide. Join us and help shape solutions that make a meaningful difference for patients around the globe.

YOUR TASKS AND RESPONSIBILITIES

* You take global responsibility for all nonclinical safety issues affecting the quality of our portfolio of marketed products, including the assessment of impurities and extractables/leachables, thereby contributing to patient safety worldwide

* You derive health-based exposure limits such as PDEs for cleaning validation and occupational safety limits, while supporting production teams on segregation concepts and worker safety requirements

* A key part of your role is ensuring Bayer's compliance across the portfolio by providing toxicological expertise for manufacturing, occupational safety and quality-related topics

* You develop integrated testing strategies to characterize the safety profile of substances in accordance with various regulatory requirements, including Medical Device Regulation

* Scientific oversight of toxicological in vitro and in vivo studies conducted at external CROs and evaluation the resulting data is a core aspect of your role

* Your expertise supports interactions with health authorities and contributes to successful regulatory processes across different regions.

* You provide scientific peer review and ensure a high level of scientific quality, rigor and regulatory compliance across projects.

WHO YOU ARE

* You hold a university degree in medicine, veterinary medicine, pharmacy, chemistry or another natural science discipline, preferably complemented by a PhD, MD or equivalent qualification.

* You bring more than five years of relevant pharmaceutical industry experience, including several years in toxicology related to marketed products and occupational toxicology.

* Developing integrated strategies for substance characterization and supporting regulatory compliance across different regulatory frameworks is within your skillset

* You have proven experience collaborating with external partners and cross-functional stakeholders, combined with strong organizational skills.

* Analysis of complex, high-volume and sometimes contradictory information while maintaining a customer-focused and solution-oriented approach comes easily to you

* Strong project management capabilities, problem-solving skills and the ability to build effective networks define the way you work in dynamic environments.

* You are skilled at structuring and steering complex processes while aligning multiple stakeholders across different organizational levels.

* Fluency in English (written and spoken) and present scientific topics clearly and effectively

WHAT WE OFFER

Our benefits package is flexible, appreciative, and tailored to your lifestyle, because: What matters to you, matters to us!

* We ensure your financial stability with a competitive salary between 109.800 EUR and 138.500EUR per year (full-time) plus a variable component and a global equity-based cash plan. Your compensation is based on your qualifications, skills, and professional experience.

* Whether it's hybrid work models or part-time arrangements: Whenever it is possible, you will have the flexibility to work how, when and where it is best for you.

* Your family is a top priority. We offer loving company daycare centers at multiple locations, support in finding childcare, time off for the care of elderly or dependent family members, summer camps for children, and much more.

* We support your professional growth by providing access to learning and development opportunities, training programs through the Bayer Learning Academy, development dialogues, as well as coaching and mentoring programs.

* We promote health awareness and opportunities for selfcare through various measures, such as free health checks with the company doctor.

* We embrace diversity by providing an inclusive work environment in which you are welcomed, supported, and encouraged to bring your whole self to work.

Be You. Be Bayer.

#LI-AMSEMEA

YOUR APPLICATION

This is your opportunity to tackle the world's biggest challenges with us: Maintaining our health, feeding growing populations and slowing the rate of climate change. You have a voice, ideas and perspectives and we want to hear them. Because our success begins with you. Be part of something big. Be Bayer.

Bayer welcomes applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.

Location: ​​ ​ Berlin or Wuppertal-Aprath​

​​Division: ​ Pharmaceuticals​

Reference Code: 875684​