480 Toxicology Jobs - Page 4

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 ...

Position Description Business Division: CreAgro Department: Biology Location: Udaipur Position Title: Research Scientist – Invitro biology (Toxicology) Level: E1-E4 Reporting to (Title): Group Leader - Invitro Biology Position Purpose The role holder shall report to the Group Leader and shall be responsible for propagation and maintanace of of cell lines & testing new active ingredients against them for the purpose of characterising the molecules for its toxic nature and advancing the identified leads from the discovery to pre-development / development of innovative chemicals for crop protection / crop growth with an aim of adding significant value to the business of PI. Strategic Responsibi...

Adviser/ Trainer for safety products and chemical risk management Main Office: Mumbai Parel Office: Home office Zone covered : Gujarat ONLY THE APPLICANTS WHO FILLED THE FORM WILL BE CONCIDERED https://forms.gle/zxvtzv2PjTdKaQMS7 ABOUT PREVOR - HSE Solutions PREVOR, a French laboratory, has been focusing for the past 60 years on researching toxicology and developing unique solutions to manage chemical risks. Our main achievement is Diphoterine®, a unique, patented first aid solution which, when used right after a chemical splash (acids & alkalis, reducing and oxidizing, chelating agents, and solvents), can significantly mitigate the severity of a burn, and deactivate all chemical reactions. ...

Job Summary The role is part of the Global Regulatory Function, responsible to prepare qualitative, error free product registration dossiers for different geographies. Job Responsibilities Compiling, organizing, and reviewing documentation required for regulatory submissions. Ensuring compliance with relevant regulations and guidelines, collaborating with cross-functional teams, and managing timelines to meet submission deadlines. Attention to detail, knowledge of regulatory requirements, and effective communication skills are crucial for success in this role. Required Education And Experience Min 5 years of relevant experience in Agri industry M.Sc. (Agriculture, Chemistry, Toxicology) MS o...

Sphera is a leading global provider of enterprise software and services that enables companies to manage and optimize their environmental, health, safety and sustainability. Our mission is to create a safer, more sustainable and productive world. Sphera is a portfolio company of Blackstone, a U.S.-based alternative asset investment company that focuses on private equity, technology and innovation, and more. Blackstone businesses succeed through strong partnerships, a personalized approach and a commitment to exceptional performance with uncompromising integrity. Sphera and Blackstone are leaders in the Environmental, Social and Governance (ESG) space. We are guided by our core values of Cust...

• Perform necropsy, gross pathology, histopathology in rodents & non-rodent toxicology studies • Act as study pathologist for toxicity studies in rodents and/or non-rodents. Required Candidate profile Prepare and/or review histopathology reports, correlation and discussion of histopathology findings in relation to clinical pathology data and/or in-life parameters

Key Skills: Exposure of various process equipment’s like Reactors (SS, MS, GLR), various type of Pumps, Dryers (FBD, Tray Dryers, VTD, RVD), Filters (Micron Filters, Sparkler Filter, PNF ), Vacuum Pumps etc., ¿ Provide operational support in development, clinical trials, toxicology study, pilot Bioequivalence batches etc. ¿ Working as shift in charge and responsible for all production activities. ¿ Preparation of daily production report. ¿ Maintain all documents related production activities. ¿ Ensure Raw Material stock availability as per plans. ¿ Preparation of qualification reports of old and new equipment’s ¿ Preparation of Development reports from available data during development Batch...

As an experienced individual with a background in M. Pharm (Pharmacology / Pharmaceutical Analysis) / M.Sc. (Biochemistry / Pharmaceutical Chemistry) with 11-14 years or Ph.D. with 2-5 years of relevant experience, you will be responsible for the following key roles and responsibilities: - Expertise in designing and executing DMPK studies to support antibody-drug conjugate (ADC) and monoclonal antibody (mAb) programs, covering the entire spectrum from discovery through IND-enabling stages. - Extensive experience in quantifying biologics such as antibodies, therapeutic proteins, ADCs, and peptides using platforms like LC-MS/MS, MSD, and ELISA. - Proficiency in utilizing advanced bioinformatic...

Learning the operations of Analytical Instruments under the guidance of mentor. Learning the new Analytical Techniques used in Analytical Research Department. Coordination with Synthesis and other cross-functional departments. To ensure Good Laboratory & safety practices in the lab. Participate in ARD SOP trainings and other departmental trainings (Quality Assurance & EHS, HRD etc) as and when required. Basic knowledge of instrumental technique with its application. Analytical chemistry (HPLC/LCMS/NMR or purification) Qualification: - M. Sc (Analytical Chemistry) Experience Any kind of internship or course work done at some Industry or reputed institute

As a Toxicology and Ingredient Data Maintenance Analyst at Colgate-Palmolive, you will play a crucial role in maintaining the accuracy and integrity of product ingredient data to ensure compliance with global regulations. Your responsibilities will include managing and updating ingredient databases, collaborating with Research & Development and Supply Chain teams, conducting risk assessments, and providing toxicological support for product development and innovation. Additionally, you will be expected to respond to internal and external inquiries regarding product safety and ingredient information, ensuring data accuracy and consistency across various products and platforms. Adapting to the ...

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a p...

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a p...

Job Summary We are looking for a dynamic and experienced Scientist to join our Pre-clinical team. This role supports the cross functional teams in product introduction, nonclinical development of generics, complex generics and differentiated products from strategy and development to product approval, across all verticals and global markets. Roles & Responsibilities You will be responsible for Preparation of Toxicological Risk Assessments, Permissible Daily Exposure and Occupational Exposure Limit monographs Tox risk assessments for excipients, impurities, extractable, leachables. You will be responding to queries regarding toxicological hazards from various cross functional teams and support...

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolve...

Company Description KGH is a not-for-profit multi-specialty hospital serving the greater Coimbatore community for over 50 years under the dynamic leadership of Chairman, Padmashri Dr. G. Bakthavathsalam. Recognized for its advanced healthcare services and commitment to charity, KGH was the first to introduce several pioneering medical technologies in the region. It is a high-volume transplant center, noted for its minimally invasive cardiac surgeries. The hospital has received numerous accolades for its contributions to medical research, education, and community health. Role Description This is a full-time on-site role for a Sr. ID. Clinical Pharmacologist located in Coimbatore. The Clinical...

Job Description About Unilever With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people – we believe that when our people work with purpose, we will create a better business and a better world. At Unilever, your career will be a unique journey, grounded in our collaborative, and flexible working environment. Our organizati...

About Unilever With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people – we believe that when our people work with purpose, we will create a better business and a better world. At Unilever, your career will be a unique journey, grounded in our collaborative, and flexible working environment. Our organizational ambition ce...

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a p...

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. : Department - Discovery Qualification - MSC - Organic Chmeistry Role - Trainee Mode - Internship Stipend - 16000 Location - Hyderabad Qualifications MSC - Organic Chemistry

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. : Medicinal chemistry; Research and development; Literature search; Scifinder / Reaxys; Design and synthesis; combiflash/Biotage; C-C coupling etc Qualifications MSC - Organic Chemistry.

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. Job description: Planning/performing and reporting of acute toxicology studies Assist in preparation of SOP"™s, Protocols and Reports Participate in GLP / AAALAC related activities Literature search Maintenance of animal house and relevant documents as per GLP and AAALAC norms. To Assist and work along with SD and TC in Plann...

Role & responsibilities Strong domain knowledge of protein biochemistry Experience in working with antibody development Understanding of structural biology with focus on protein and antibody Publications in scientific peer reviewed journals Excellent scientific writing skills Proficient in bioinformatics tools specially used in protein engineering/molecular biology A good understanding and hands-on experience in proteomics data analysis Laboratory working experience in immunology and protein biochemistry Familiarity with molecular biology, genomics and structural biology concepts is preferred Ability to adapt to new challenges and fast-paced research environment Willingness to learn new topi...

Job Title: Senior Executive – Regulatory Affairs Industry: Pharmaceuticals Experience Required: 3–5 Years Job Summary: We are seeking a detail-oriented and proactive Senior Executive – Regulatory Affairs to ensure compliance with regulatory standards applicable to pharmaceutical products. The role involves managing end-to-end regulatory submissions, monitoring compliance with REACH, FSSAI, CDSCO , and other relevant national and international guidelines. Key Responsibilities: Prepare, review, and maintain dossiers, Product Information Files (PIFs), SDS,COAs, toxicological reports, CPSRs, and compliance statements. Manage global regulatory submissions and compliance for international countrie...

Company Description Trishveda Naturals Pvt Ltd specializes in producing a wide range of specialized oils and powders from fruits, vegetables, flowers, minerals, and seeds using a physical manufacturing process. These natural ingredients have diverse applications in various beauty and personal care products. Utilizing plant-based chemistry and biotechnology platforms, Trishveda Naturals develops high-value products, innovations, and new functions with natural ingredients. Job Title: Senior Executive – Regulatory Affairs Industry: Pharmaceuticals Experience Required: 3–5 Years Job Summary: We are seeking a detail-oriented and proactive Senior Executive – Regulatory Affairs to ensure compliance...

Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their labora...