Senior Toxicologist Vipragen Biosciences Pvt Ltd

8.0 - 12.0 years

5 - 15 Lacs

Mysuru

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Position: Senior Toxicologist Location: Mysore, Karnataka Experience: 8 to 15 years About Us: Vipragen Biosciences Pvt ltd is a leading organization specializing in drug discovery and development services. We are committed to advancing scientific research and innovation through cutting-edge technology and a collaborative work environment. Industry: Preclinical CRO (GLP-OECD certified) About the Role: Vipragen Bioscience Pvt Ltd is seeking an experienced and highly skilled Toxicologist to join our growing team at our OECD GLP-certified preclinical CRO in Mysore. The ideal candidate will be responsible for conducting and overseeing in vivo repeated dose toxicity studies for global regulatory submissions. Candidates with a DABT certification will be preferred. Key Responsibilities: Independently design, conduct, and interpret in vivo repeated dose toxicity studies for regulatory submissions across the globe (FDA, OECD, EU, REACH, etc.) Select appropriate doses and determine PoDs (NOEL, NOAEL, STD10) based on preclinical toxicology results Ensure all preclinical research and reports comply with GLP , OECD , ICH , Indian Schedule Y , and other global regulatory guidelines Contribute to pre-clinical/non-clinical development plans , including study design, data interpretation, and strategy support for pharmaceuticals, agrochemicals, biotechnology products, and medical devices Provide risk assessment and regulatory support to ongoing R&D projects Lead and mentor a team of 510 toxicology professionals , providing guidance and support throughout the study lifecycle Resolve study-related, regulatory, and client-related issues in a timely and compliant manner Collaborate effectively with cross-functional teams including Sponsors/Clients, Business Development, Project Management, and Technical Teams Participate in on-site and telecon meetings to support client interactions and study updates Preferred Qualifications: M.sc / Ph.D. in Toxicology, Pharmacology, or related life sciences field DABT Certification (preferred) Proven expertise in preclinical toxicology , risk assessment , and regulatory submissions Strong knowledge of GLP , OECD , FDA , EU , REACH , and IND requirements Excellent communication, leadership, and problem-solving skills Willingness to relocate to Mysore Desired Qualities: Problem-Solving: Strong problem-solving skills with a proactive approach to addressing technical challenges. Innovative Thinking: Ability to think critically and creatively to develop and implement new methodologies. Time Management: Effective time management skills to balance multiple projects and meet deadlines. Adaptability: Flexibility to adapt to changing priorities and project requirements. What We Offer: Competitive salary and benefits package Opportunities for professional development and career advancement A dynamic and inclusive work environment Access to state-of-the-art research facilities and technology Application Process: Interested and qualified candidates are invited to apply by sending their updated resume to: hr@vipragen.com Vipragen is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Posted 3 weeks ago

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Principal Scientist - Study Director Toxicology Eurofins Advinus

7.0 - 10.0 years

6 - 16 Lacs

Bengaluru

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Job Title: Principal Scientist - (Study Director in Toxicology) Location: Bangalore Industry: Pre-clinical Contract Research Organization Job Type: Full-time About the Role: We are seeking an experienced Principal Scientist to lead our toxicology studies, designing, conducting, and reporting non-clinical safety studies (GLP and non-GLP) in support of drug development and regulatory submissions. This role demands strong scientific leadership, regulatory expertise, and cross-functional collaboration. Key Responsibilities: Design, conduct, and report non-clinical safety studies (GLP and non-GLP) for drug development and regulatory submissions. Provide scientific leadership and ensure regulatory compliance in toxicology studies. Collaborate with cross-functional teams to ensure study integrity and success. Requirements: Experience: 8-10 years of relevant experience in toxicology or a related field. Education: Ph.D. or Master's degree in Veterinary Sciences or Biosciences. Desirable Certifications: DABT Certification and FELASA certification. Skills: Expertise in repeat dose toxicity, teratology, and reproductive toxicity experimentation. Strong understanding of pharmaceutical R&D and agrochemical testing processes. Excellent team working and leadership skills. In-depth knowledge of GLP and regulatory guidelines. Strong scientific writing and communication skills. Ability to manage multiple projects and lead teams. Proficiency in data analysis and interpretation. Behavioral Competencies: Excellent communication and adaptability. Effective time management. Continuous learning and improvement. Structured work approach. What We Offer: Opportunity to work in a dynamic CRO environment. Collaborative team. Growth opportunities. If you are a motivated professional looking to lead in toxicology, apply now with your resume. How to Apply: Email: Sekhar.Sompalli@advinus.eurofinsasia.com

Posted 1 month ago

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