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15.0 - 20.0 years
0 Lacs
karnataka
On-site
As a Section Head - Toxicology at Eurofins Advinus Private Limited, you will be responsible for leading key regulatory toxicology studies, mentoring and developing scientific teams, and driving strategic initiatives in drug development programs. With over 30 years of GLP experience, Eurofins Advinus is a premier contract research, development, and manufacturing organization serving diverse industries. **Key Responsibilities:** - Lead key regulatory toxicology studies - Mentor and develop scientific teams - Drive strategic initiatives in drug development programs **Qualifications Required:** - 15-20 years of relevant experience - Ph.D. or Masters in Veterinary Sciences or Biosciences - Certif...
Posted 3 weeks ago
10.0 - 15.0 years
35 - 50 Lacs
navi mumbai
Work from Office
JOB SUMMARY: Knowledgeable in all disciplines of ecotoxicology, including aquatic, plants, avian, mammals, and terrestrial. Conduct ecotoxicological risk assessments and provide expert guidance to internal colleagues on ecotoxicology issues, including responses to Regulatory decisions, Data Call In reviews and recommendations, and planning defense strategies around ecotoxicology concerns. Experience with interacting with regional Regulatory Agencies especially US-EPA and European Authorities. Familiar with global data requirements, including North America, Brazil, LATAM, and Europe. Contract ecotoxicology studies at external labs. Interpret study results and implications of results. Provide ...
Posted 1 month ago
0.0 years
4 - 6 Lacs
hyderabad, telangana, india
On-site
Provide comprehensive contract research services in drug discovery, preclinical, and early development stages. Conduct regulatory toxicology studies for safety assessment to support drug development pipelines. Perform DMPK (Drug Metabolism and Pharmacokinetics) studies to evaluate ADME (Absorption, Distribution, Metabolism, and Excretion) profiles of drug candidates. Deliver Analytical R&D services including method development, validation, and stability studies for early-stage drug substances. Support API CDMO (Active Pharmaceutical Ingredient Contract Development and Manufacturing Organization) operations, focusing on manufacturing drug substances for toxicology and early clinical studies. ...
Posted 1 month ago
2.0 - 6.0 years
0 Lacs
kolkata, west bengal
On-site
As a Regulatory Toxicology & Pharmacology professional in Kolkata, you will be expected to have a clear understanding of Regulatory Toxicology & Pharmacology principles with robust domain knowledge. Additionally, you should possess a good understanding of OECD guidelines Safety Guidelines and be familiar with risk assessment, Hazard assessment, Exposure assessment & Safety assessment. Your role will also require knowledge of various Toxicology/ Pharmacology/ clinical/ Regulatory databases and dose calculation & conversions. With 2-3 years of experience, you should have the capability of interpretation of results and analysis of key toxicity data. Qualifications required for this position inc...
Posted 1 month ago
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