483 Toxicology Jobs - Page 18

JOB DESCRIPTION Jubilant Bhartia Group . About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared) in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutica...

Synthesis, purification, and characterization of novel intermediates. Deliver small to large quantities of by novel chemical entities for drug discovery. Work collaboratively in a team to drive chemistry projects forward. Responsible for safe conduct of reactions. Excellent knowledge in basic and advance organic chemistry. Good knowledge in functional group conversion and multiple step synthesis Basic knowledge retrosynthetic analysis (desirable). Good expertise in handling pyrophoric reactions. Good knowledge of TLC, column purification, extraction. Excellence in analysing NMR, IR and Mass Spectrometry data. Always adhere to safe laboratory practices. Enthusiasm to work in a dynamic researc...

Synthesis, purification and characterization of novel chemical compounds. Deliver small to large quantities of by novel chemical entities for drug discovery. Work collaboratively in a team to drive chemistry projects forward. Responsible for safe conduct of reactions. Excellent knowledge in basic and advance organic chemistry. Good knowledge in functional group conversion and multiple step synthesis. Basic knowledge retrosynthetic analysis (desirable). Good expertise in handling pyrophoric reactions. Good knowledge of TLC, column purification, extraction. Excellence in analyzing NMR, IR and Mass Spectrometry data. Always adhere to safe laboratory practices. Enthusiasm to work in a dynamic re...

JOB DESCRIPTION Jubilant Bhartia Group . About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared) in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutica...

The Position: Organization: - Jubilant Ingrevia Limited Designation & Level: - Dy/Manager Regulatory Affairs Location: - Greater Noida Reporting Manager: - Head QA & RA The Structure: Job Summary: To maintain compliance scheme for both Domestic & International regulations like EU REACH, , with other REACH-like regulations of specialty chemicals, as well DMF filing, life cycle management of active ingredients /supplements category. As the Regulatory Compliance Manager, you will be accountable for leading product regulatory activities in the various region through monitoring, developing and implementing strategies/programs to ensure compliance with the required chemical control laws. Job Respo...

Job Title: Product Stewardship Specialist II - Regulatory Services Summary: This position is responsible for Product Stewardship Regulatory services around dossier preparation and submission (e.g. EU-REACH, UK-REACH, KKDIK, etc.). Establish and maintain processes (e.g. e-SDS, C&L notifications, Trade secret Notifications). Effective coordination between internal and external functions and stakeholders. The role covers the activity for products from all Business Segments, ensuring continuity and growth of these businesses through compliance with regulations. Works directly with all levels within Momentive businesses and direct resources, with appropriate expertise in supporting Substance/prod...

Job Title: Advanced Product Steward - Regulatory Services Summary: This position is responsible for Product Stewardship Regulatory services around dossier preparation and submission (e.g. EU-REACH, UK-REACH, KKDIK, etc.). Establish and maintain processes (e.g., e-SDS, C&L notifications, Trade secret Notifications). Effective coordination between internal and external functions and stakeholders. The role covers the activity for products from all Business Segments, ensuring continuity and growth of these businesses through compliance with regulations. Works closely with the Business Teams with the focus on Substance/product registration strategy and execution to support new product development...

Company Description Syngenta is one of the world’s leading agriculture innovation company (Part of Syngenta Group) dedicated to improving global food security by enabling millions of farmers to make better use of available resources. Through world class science and innovative crop solutions, our 60,000 people in over 100 countries are working to transform how crops are grown. We are committed to rescuing land from degradation, enhancing biodiversity and revitalizing rural communities. A diverse workforce and an inclusive workplace environment are enablers of our ambition to be the most collaborative and trusted team in agriculture. Our employees reflect the diversity of our customers, the ma...

Company Description: Rohana Veterinary Diagnostic Lab (RVD) is Bengaluru’s first lab with state of art Veterinary diagnostic technology and exclusively catering to the ever-increasing needs of Veterinary population. Through RVD, we offer quality diagnostic services like routine hemogram, serum biochemistry, immunology, bacteriology, serology, virology, histopathology, parasitology, analytical services, molecular diagnostics and toxicology for animal species. Role Description: This is a full-time on-site role for a Senior Lab Technician located in Bengaluru. The Senior Lab Technician will be responsible for operating laboratory equipment, conducting quality control tests, and utilizing analyt...

The Regulatory Medical Writer collaborates with the Medical Writing team and clients to prepare high-quality regulatory documents (Investigators Brochures, Safety Narratives, protocols, investigator brochures, synopses, etc.). The Regulatory Medical Writer is responsible for providing clinical regulatory document support and scientific writing expertise to the clinical teams, ensuring successful preparation of high-quality submission-ready documents and effective implementation of the writing process. The Regulatory Medical Writer will also be responsible for the expanded development, implementation, and maintenance of operations related to clinical trial registration and results disclosure....

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com Looking to jump-start your career We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you...

Job ID: 40012 | Location: Airoli, Maharashtra, India Responsibilities Strong understanding of regulatory compliance and relevant systems. Knowledge of monitoring and interpreting dynamic regulatory changes and their impact on the portfolio. Ability to collaborate with regions/Business Units for regulatory updates and assessments. Experience in providing data for risk and impact assessments. Expertise in managing product safety data in SAP (evaluation, maintenance, archiving). Proven track record in process optimization and enhancement. Experience in Product Stewardship operations, including creation of regulatory documents. Requirements M.Sc. in Chemistry or related fields. 5+ years of exper...

- Assist in Dossier preparation and review various reports. - Coordinate with various institutes and Overseas experts on Toxicology, Efate and physiochemical part of dossiers - liaison, negotiate with labs and timely completion of studies -Chemicals Required Candidate profile Graduate or Post Graduate in Chemistry, Agriculture or Bioscience. Excellent in oral and written communication. Ability to manage complex issues and prioritize workload.

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 Title : Assistant Manager – R&D Formulation (Colour Cosmetics) Department : R&D Reporting Structure Reports to : R&D Head Roles That Report Into The Role Holder Role Location : Kheda, Gujarat India Educational Qualifications Required Must have a degree in Cosmetic Chemistry. Those with a master’s degree would be preferred. Number Of Years’ Experience Required 6 – 10 years of experience Preferences Must come from Colour Cosmetics / makeup industry (lipsticks / eyeliners / mascara / nail polish Should be a female candidate. Job Purpose To drive the formulation work for the groups makeup products. Principal Accountabilities & Responsibilities Carry out formulation development for the groups...

Job Title : Assistant Manager – R&D Formulation (Aerosols) Department : R&D Reporting Structure Reports to : R&D Head Roles That Report Into The Role Holder Role Location : Kheda, Gujarat India Educational Qualifications Required Must have a degree in Chemistry. Those with a master’s degree would be preferred. Number Of Years’ Experience Required 8 – 10 years of experience Preferences Must come from the aerosol industry (focusing on products like deodorants) Job Purpose To drive the formulation work for the group’s aerosol-based products. Principal Accountabilities & Responsibilities Carry out formulation development for the groups fragrance & aerosol brands. These will be products like; deo...

Job Title : R&D Formulation Chemist – Executive Department : R&D Reporting Structure Reports to : R&D Manager(Personal Care) Roles that report into the role holder: Nil Role Location : Kheda, Gujarat, India Educational Qualifications Required Education background in Chemistry, Chemical Engineering, Cosmetic Science is a must. Number Of Years’ Experience Required 3-5 years of experience Preferences Must be from the Personal Care industry. Job Purpose To successfully contribute towards the formulation development for a wide range of the groups personal care products. Principal Accountabilities & Responsibilities Carry out formulation development for the groups personal care brands. Define prod...

Summary The Preclinical Safety (PCS) department within the Novartis Biomedical Research - Translational Medicine Unit provides non-clinical safety strategy of products in -discovery, -development and -market, globally, with state-of-the-art regulatory compliance. As a Principal Scientist-2, you will join our PCS team in India to discuss strategies and deliver non-clinical safety deliverables for the products you are globally responsible for. This role also involves development and review of nonclinical scientific submission components (eCTD module 2.4 and 2.6) and other lifecycle management regulatory documents for multiple projects. About The Role Key Responsibilities : Strategy and deliver...

Job Title: Senior Scientist - In Vitro Secondary Pharmacology Career Level: D Introduction to role: Are you ready to make a significant impact in the world of drug discovery and developmentJoin AstraZenecas Clinical Pharmacology Safety Sciences (CPSS) department, where innovation meets collaboration. Our Safety Innovation team is at the forefront of advancing a diverse pipeline across therapeutic areas, delivering safety science from early discovery through clinical development. We are seeking a talented in vitro pharmacologist to join our Secondary Pharmacology team, contributing to the clinical advancement of new medicines. Accountabilities: In this pivotal role, youll leverage your expert...

We are looking for a Life Science Senior Content Specialist to join our team in Hyderabad/Noida . This is an amazing opportunity to work on OFF-X, a translational drug safety intelligence portal . The team consists of 20 people located in Spain and India and is reporting to the India-based Team Manager. We have a great skill set in the analysis of drug safety and toxicity data and we would love to speak with you if you have skills in that area About You - experience, education, skills, and accomplishments Degree in Life Sciences (Pharmacy, Pharmacology, Toxicology, Biology, Biomedical Sciences, etc.) Min 5 years of experience in drug safety, toxicology, pharmacovigilance Excellent English wr...

Role: Product Manager Department: DPEx Role Band: S - equivalent to Indigo Location: Miyapur, Hyderabad No. of Positions: - 01 Context: APSL has embarked on an organization wide initiative of Business Transformation Process Excellence leveraging Digital, Analytics Automation. The DPEx team plays a key role in understanding business processes, suggesting solutions and planning executing these solutions to create direct impact on business KPIs. The Product Manager is expected to lead many such initiatives within the organization. The product manager should understand the business requirements, map processes, translate business process requirements into business requirement specifications and d...

We are looking for a Life Science Senior Content Specialist to join our team in Hyderabad/Noida. This is an amazing opportunity to work on OFF-X, a translational drug safety intelligence portal. The team consists of 20 people located in Spain and India and is reporting to the India-based Team Manager. We have a great skill set in the analysis of drug safety and toxicity data and we would love to speak with you if you have skills in that area About You – Experience, Education, Skills, And Accomplishments Degree in Life Sciences (Pharmacy, Pharmacology, Toxicology, Biology, Biomedical Sciences, etc.) Min 5 years of experience in drug safety, toxicology, pharmacovigilance Excellent English writ...

Requirements Description and Requirements Basic Function The process consists of Review, research, and investigate pended Group Life claim submission with multiple coverages and complexity to determine if claim is payable in accordance with various policy provisions, manage Call-ups and outreach to groups for missing information. Essential Functions ( The key deliverables of the role will include but will not be restricted to the details below ) Identify and obtain missing information required to evaluate Group life claims and input information into a Windows based computer system (BIOS). Interpret policy provisions and manually adjudicate Group Life claims to make claim determinations. Work...

The Preclinical Safety (PCS) department within the Novartis Biomedical Research - Translational Medicine Unit provides non-clinical safety strategy of products in -discovery, -development and -market, globally, with state-of-the-art regulatory compliance. As a Principal Scientist-2, you will join our PCS team in India to discuss strategies and deliver non-clinical safety deliverables for the products you are globally responsible for. This role also involves development and review of nonclinical scientific submission components (eCTD module 2.4 and 2.6) and other lifecycle management regulatory documents for multiple projects. Key Responsibilities : Strategy and delivery of PCS deliverables f...

The Purpose of the Specialist role is having expertise in Extractables and Leachables assessment, work in close collaboration with multiple functions such as MST, Supplier management, Regulatory, Toxicology, Procurement, Quality and Production. The individual plays a key role in support of Extractable and Leachable activities with a strong focus on data collection, Risk rating, assessments and evaluation. Key Responsibilities: Extractable and Leachable (EL) Expertise Understanding of Extractable and Leachable (EL) risk assessment for materials based on supplier information and the ability to determine the risk level and update the Risk assessment. Building a comprehensive material library ba...