Hybrid Toxicology Analyst – Pharma Safety

Über das Unternehmen

Takeda Pharmaceutical Company Limited is a global, values-based, R&D-driven biopharmaceutical leader headquartered in Japan, committed to bringing Better Health and a Brighter Future to patients by translating science into highly innovative medicines. Takeda focuses its R&D efforts on four therapeutic areas: Oncology, Gastroenterology (GI), Rare Diseases, and Neuroscience. We also make targeted R&D investments in Plasma-Derived Therapies and Vaccines. Operating in approximately 80 countries and regions, Takeda is a diverse and inclusive company that empowers its employees to contribute to its mission.

Stellenbeschreibung

Join Takeda’s dedicated Pharma Safety team as a Hybrid Toxicology Analyst. In this crucial role, you will be instrumental in assessing the safety profile of our pharmaceutical products, from early development to post-market surveillance. Your expertise in toxicology will directly contribute to protecting patient health by identifying, evaluating, and mitigating potential risks associated with drug candidates and marketed medicines. This hybrid position offers the flexibility of both office collaboration and remote work, allowing you to engage with a dynamic team while managing your individual research and analysis tasks.

Hauptverantwortlichkeiten

• Conduct comprehensive toxicological risk assessments for pharmaceutical compounds.
• Analyze non-clinical safety data, including in vivo and in vitro studies, to identify potential hazards.
• Prepare detailed safety reports and summaries for regulatory submissions and internal stakeholders.
• Collaborate with cross-functional teams, including R&D, Clinical Development, Regulatory Affairs, and Pharmacovigilance.
• Monitor scientific literature and regulatory guidelines for updates relevant to toxicology and drug safety.
• Provide expert toxicological input during drug development phases and issue resolution.
• Participate in the design and oversight of toxicology studies.

Erforderliche Fähigkeiten

• Master's degree or Ph.D. in Toxicology, Pharmacology, Biochemistry, or a related life science field.
• Minimum of 3 years of experience in toxicology within the pharmaceutical or biotechnology industry.
• Strong understanding of regulatory guidelines (e.g., ICH, EMA, FDA) related to non-clinical safety.
• Proficiency in interpreting complex toxicological data and performing risk assessments.
• Excellent written and verbal communication skills in English.
• Ability to work independently and collaboratively in a fast-paced environment.

Bevorzugte Qualifikationen

• DABT (Diplomate of the American Board of Toxicology) or equivalent certification.
• Experience with global regulatory submissions.
• Knowledge of drug development processes.
• Familiarity with pharmacovigilance principles.

Vorteile & Zusatzleistungen

• Competitive salary and performance-based bonuses.
• Comprehensive health, dental, and vision insurance.
• Generous paid time off and holidays.
• Pension scheme with company contribution.
• Professional development and training opportunities.
• Hybrid work model flexibility.
• Access to an on-site fitness center and wellness programs.
• Employee assistance program.

Jetzt bewerben