356 Toxicology Jobs

Company Description Dabur Research Foundation (DRF), established in 1979, is an Indian Contract Research Organization offering preclinical services for Drug Discovery and Development. Operating independently since 2008, DRF provides services across In Vitro, Ex-Vivo & In Vivo Pharmacology, Exploratory & GLP Toxicology, and DMPK. With over 30 years of experience, we support global Biotech, Pharma, Phytopharmaceuticals, Cosmeceuticals, and academic sectors through every step of drug discovery and development. Role Description We are looking for a GLP QA Inspector (full-time, on-site, South Delhi). The role involves monitoring and ensuring compliance with Good Laboratory Practices (GLP) in preclinical studies. Responsibilities include conducting audits, reviewing study documentation, ensuring adherence to protocols, and supporting GLP standards across study processes. Qualifications Bachelor’s or Master’s degree in Life Sciences, Biotechnology, Pharmacology, Chemistry, or related field 2–4 years of QA experience in a GLP environment (preclinical research experience preferred) Strong understanding of regulatory guidelines and protocols (OECD GLP Guidelines) Experience in audits, inspections, and compliance monitoring Excellent organizational, written, and verbal communication skills Ability to work independently and collaboratively How to Apply Please send your CV to hr@daburresearch.in with the subject line Position_Name .

Company Description Acutis Diagnostics is a laboratory medicine company specializing in clinical toxicology and breakthrough branded molecular diagnosis. We are committed to combining hard science and technology with the expertise of our highly skilled professionals. We believe in accessible benefits for all team members and have built a company with no gaps or bureaucracy. Our latest offering is Acutis Reveal™ molecular tests for infectious diseases, which we are introducing to healthcare professionals. Role Description This is a full-time remote role for a Fleet Service Coordinator at Acutis Diagnostics. The Fleet Service Coordinator will be responsible to manage our fleet of drivers who are responsible for collecting samples for laboratory testing. The ideal candidate will have a strong background in logistics management, excellent communication skills, and proficiency in fleet management software. This role requires constant availability to communicate with drivers and handle any logistical challenges that may arise. Responsibilities: Coordinate and oversee the daily operations of the driver fleet, ensuring timely sample pickups and deliveries. Utilize fleet management software to track driver locations, schedules, and performance metrics. Communicate effectively with drivers to provide instructions, updates, and support as needed. Monitor route efficiency and adjust optimize delivery schedules and minimize delays. Collaborate with other departments to ensure seamless coordination between sample collection, transportation, and laboratory processing. Resolve any issues or conflicts that may arise during transportation, including vehicle maintenance, traffic delays, or customer concerns. Maintain accurate records of all transportation activities, including driver logs, mileage, and fuel consumption. Implement and enforce safety protocols to ensure compliance with transportation regulations and company policies. Provide training and support to drivers to enhance their performance and professionalism. Stay informed about industry trends and best practices in logistics management to continuously improve processes and efficiency. Qualifications: Bachelor's degree in Logistics, Supply Chain Management, Business Administration, or related field preferred. Minimum of 3 years of experience in logistics coordination, preferably in a transportation or delivery-related industry. Proficiency in fleet management software (e.g., GPS tracking, route optimization) and Microsoft Office Suite. Strong communication skills, both verbal and written, with the ability to effectively interact with drivers, clients, and internal teams. Excellent problem-solving abilities and the capacity to handle multiple tasks simultaneously in a fast-paced environment. Detail-oriented with a focus on accuracy in record-keeping and data analysis. Availability to be on-call and respond to logistical issues outside of regular business hours. Knowledge of transportation regulations and safety standards. Leadership skills with the ability to motivate and support a team of drivers to achieve company goals. Adaptability and willingness to embrace change and implement new strategies for improved efficiency.

Job Title: Laboratory Technician – Urine Toxicology Screening Location: Remote Company Overview: We are a growing healthcare organization committed to providing accurate, timely, and reliable diagnostic services. Our team values precision, professionalism, and dedication to patient care. Position Summary: We are seeking a qualified and detail-oriented Laboratory Technician to join our team. The ideal candidate will have hands-on experience in performing urine toxicology screenings, analyzing reports, and ensuring accurate documentation. Key Responsibilities: Perform urine toxicology screenings following standard protocols. Operate, calibrate, and maintain laboratory equipment. Accurately analyze and interpret results of toxicology tests. Prepare and maintain detailed laboratory reports. Ensure compliance with quality control and safety standards. Collaborate with physicians and other healthcare professionals regarding test results. Qualifications: Bachelor’s degree in Medical Laboratory Technology, Biochemistry, Microbiology, or a related field. Proven experience in running urine toxicology screenings and preparing reports. Strong knowledge of laboratory protocols, safety, and quality assurance. Attention to detail, accuracy, and organizational skills. Ability to work independently and as part of a team. Preferred Skills: Experience with advanced toxicology analyzers and lab software. Familiarity with accreditation standards and regulatory guidelines. Compensation & Benefits: Competitive salary (commensurate with experience). Health and insurance benefits. Opportunities for career growth and professional development. How to Apply: Interested candidates may send their CV and cover letter to careers@paintreatmentmd.com with the subject line “Application – Laboratory Technician.” Job Type: Full-time Pay: From ₹40,000.00 per month

As a Doctor in Forensic Medicine at our premier leading Medical College & Research Centre in Chennai, you will be responsible for contributing to academic excellence through teaching, training, research, and medico-legal expertise in the Department of Forensic Medicine. **Key Responsibilities:** - Teach undergraduate (MBBS, BDS, Nursing, Allied Health Sciences) and postgraduate students in Forensic Medicine & Toxicology. - Conduct lectures, practical sessions, autopsy demonstrations, seminars, and tutorials. - Guide PG students in dissertation work, case discussions, and journal clubs. - Integrate forensic principles with clinical and legal practice. - Update curriculum and teaching materials as per NMC guidelines. - Undertake and guide original research projects in forensic pathology, toxicology, medical jurisprudence, and allied fields. - Publish in reputed national and international indexed journals. - Collaborate with other medical and legal departments for interdisciplinary research. - Support Ph.D. scholars and PG thesis work. - Supervise and conduct medicolegal autopsies and postmortem examinations. - Provide expert medico-legal opinion in criminal and civil cases. - Ensure proper documentation, preservation of samples, and medico-legal record maintenance. - Liaise with police, judiciary, and forensic science laboratories as required. - Organize academic events such as CMEs, workshops, and training programs. - Manage departmental records, museum specimens, and laboratory facilities. - Ensure adherence to ethical, legal, and institutional policies. - Serve as Head/Coordinator of the Department (for Professors). **Qualifications & Experience:** - Professor: MD (Forensic Medicine) with at least 8 years teaching experience, including 3 years as Associate Professor (as per NMC norms), plus research publications. - Associate Professor: MD (Forensic Medicine) with at least 5 years teaching experience, including 2 years as Assistant Professor, plus research publications. - Assistant Professor: MD (Forensic Medicine) with teaching/research experience as per NMC requirements; publications desirable. In this role, it is essential to possess strong academic, clinical, and medico-legal knowledge, excellent teaching and mentoring abilities, research aptitude with a publication track record, ability to provide medico-legal expertise with accuracy and integrity, and effective communication and collaboration skills with law enforcement and judiciary.,

Preparation of study plan considering the client requirements as well as regulatory requirements. Preparing a study schedule and communicating with all the study personnel and ensuring the proper conduct of the study. Preparing reports after completion of each study. This involves evaluating the data output by applying scientific knowledge and skills. To maintain the highest regulatory standards (OECD GLP) during any activity conducted in the facility by continuous monitoring and checkup of all the instruments/equipment used in a study as per Standard Operating Procedures (SOPs). Preparation and periodic revision of Standard Operating Procedures. Preparation and presentation of experiment conduct protocols to the Institutional Animal Ethics committee. Periodically verify data generated during study. Archival of the study plan, study report, raw data and related materials as per the study plan. Coordinate with TFM and/or study personnel and keeping informed of their findings during the study and receipt and evaluation of their respective individual reports for inclusion in the final study report.

Job Description Key role requirements for this position: **Expert Knowledge in Forensic Medicine**: Deep understanding of forensic pathology, toxicology, and clinical forensic medicine is essential. The professor should stay current with advances in the field and have practical experience in medico-legal investigations. **Teaching and Curriculum Development**: Develop and deliver comprehensive educational programs for students in forensic medicine. This includes designing course content, creating lectures, and developing practical training modules. **Research and Publication**: Conduct original research in forensic medicine, publish findings in peer-reviewed journals, and contribute to the advancement of the field. This also involves securing research funding and leading research projects. **Supervision and Mentoring**: Supervise and mentor students, postgraduate researchers, and junior faculty. Provide guidance on academic, research, and career development. **Professional Practice**: Engage in forensic practice by providing expert testimony in legal settings, consulting on medico-legal cases, and working with law enforcement and legal professionals. **Academic Leadership**: Contribute to the academic leadership of the department or faculty, including participating in committees, developing strategic plans, and contributing to accreditation processes. **Interdisciplinary Collaboration**: Work with professionals from other disciplines such as law, psychology, and criminology to foster interdisciplinary approaches and enhance the educational and research environment. **Continuing Education and Training**: Participate in ongoing professional development and continuing education to stay updated with the latest advancements in forensic medicine and related fields. Academic Qualifications: MBBS+MD(Forensic Science) Full time 3800k Year Forensic Medicine Forensic Medicine Full time 3800k Year

Kenvue Is Currently Recruiting For A: Principal Scientist What We Do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role Reports To: 总监,毒理 Location: Asia Pacific, India, Maharashtra, Greater Mumbai Work Location: Fully Onsite What You Will Do Kenvue is currently recruiting for: Principle Scientist-Toxicology & Clinical Safety (skin tolerance) Who We Are At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including Neutrogena, Aveeno, Tylenol, Listerine, Johnson’s and BAND-AID® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse and brilliant people, passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact the life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Location : Mumbai What You Will Do Kenvue has products in beauty, baby, oral care, topical healthcare, personal hygiene and OTC franchises. Toxicology Resource Centre is engaged in the conduct of safety assessment of ingredients and products. This position entails conducting toxicology risk assessments for ingredients, finished products, impurities, and degradants, as well as evaluating topical skin safety for consumer products through data research and interpretation. It does not involve any laboratory work. Additionally, the role requires monitoring studies at Contract Research Organizations (CROs). Candidates should possess qualifications in Toxicology or Clinical Safety, along with experience in conducting in vitro or in vivo toxicology studies and/or skin tolerance studies, as well as risk assessment and medical writing skills. Responsibilities also include coordinating with third-party contractors, reviewing activities and assessments, mentoring junior scientists, and representing the team in technical and strategic discussions. Strong communication skills are essential for successful job performance. Job Responsibilities: Literature search and scientific data collection for preparation of hazard assessment report of the cosmetic ingredients Assessment of ingredients/raw materials/formulae at different stages of product development in skin care, essential health franchise Preparation of APR statements/Tox clearance statements and other relevant documents such as CPSRs, CCDS to support regional regulatory requirements as and when required Safety assessment of fragrances and flavors used in consumer products Preparation/Updating of INCI tox profiles The Principal Scientist (Toxicology/Clinical Safety) represents toxicology/safety in essential health and/or skin care franchise project teams and works with cross-functional business partners, PD team, RMC, the formulators, and suppliers etc. on a regular basis for obtaining more details regarding RMs, fragrances, formulas etc. to establish their pre-clinical safety strategies and perform their timely safety assessments in support of project timelines. Review of Assessment reports prepared by other Scientists and their approvals Representing AP tox team to attend global strategic discussion meeting on clinical safety Representing AP tox team to attend TRC discussion meeting. Mentoring junior scientist What We Are Looking For Master’s degree/ Ph.D. in toxicology, pharmacology or relevant science discipline. >3 years of experience in the field of consumer product risk assessment or other relevant Toxicology and/or Clinical safety (skin tolerance) experience. Diplomate of the American Board of Toxicology (DABT) certification, Diploma in clinical sciences preferred. In silico predictions Good verbal and written communication skill in English is a must. Individual with strong interpersonal skills and able to work independently Desirable: Knowledge of regulatory requirements for product safety submissions and experience in medical writing. What’s In It For You Competitive Benefit Package* Paid Company Holidays, Paid Vacation, Volunteer Time & More! Learning & Development Opportunities Employee Resource Groups This list could vary based on location/region Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process. Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Company Description Acutis Diagnostics is a laboratory medicine company specializing in clinical toxicology and breakthrough branded molecular diagnosis. We are committed to combining hard science and technology with the expertise of our highly skilled professionals. We believe in accessible benefits for all team members and have built a company with no gaps or bureaucracy. Our latest offering is Acutis Reveal™ molecular tests for infectious diseases, which we are introducing to healthcare professionals. Role Description This is a full-time remote role for a Fleet Service Coordinator at Acutis Diagnostics. The Fleet Service Coordinator will be responsible to manage our fleet of drivers who are responsible for collecting samples for laboratory testing. The ideal candidate will have a strong background in logistics management, excellent communication skills, and proficiency in fleet management software. This role requires constant availability to communicate with drivers and handle any logistical challenges that may arise. Responsibilities: Coordinate and oversee the daily operations of the driver fleet, ensuring timely sample pickups and deliveries. Utilize fleet management software to track driver locations, schedules, and performance metrics. Communicate effectively with drivers to provide instructions, updates, and support as needed. Monitor route efficiency and adjust optimize delivery schedules and minimize delays. Collaborate with other departments to ensure seamless coordination between sample collection, transportation, and laboratory processing. Resolve any issues or conflicts that may arise during transportation, including vehicle maintenance, traffic delays, or customer concerns. Maintain accurate records of all transportation activities, including driver logs, mileage, and fuel consumption. Implement and enforce safety protocols to ensure compliance with transportation regulations and company policies. Provide training and support to drivers to enhance their performance and professionalism. Stay informed about industry trends and best practices in logistics management to continuously improve processes and efficiency. Qualifications: Bachelor's degree in Logistics, Supply Chain Management, Business Administration, or related field preferred. Minimum of 3 years of experience in logistics coordination, preferably in a transportation or delivery-related industry. Proficiency in fleet management software (e.g., GPS tracking, route optimization) and Microsoft Office Suite. Strong communication skills, both verbal and written, with the ability to effectively interact with drivers, clients, and internal teams. Excellent problem-solving abilities and the capacity to handle multiple tasks simultaneously in a fast-paced environment. Detail-oriented with a focus on accuracy in record-keeping and data analysis. Availability to be on-call and respond to logistical issues outside of regular business hours. Knowledge of transportation regulations and safety standards. Leadership skills with the ability to motivate and support a team of drivers to achieve company goals. Adaptability and willingness to embrace change and implement new strategies for improved efficiency.

Ashland India Private Ltd Are you the kind of person that is always thinking, sketching, seeking, and adjusting? Who needs to understand how things work and then figure out how they can work better? Are you a passionate, tenacious, solver who loves to work with others who share your drive? Are you positive, constructive, and ingenious? Are you always solving? Then we’d like to meet you and bet you’d like to meet us. Ashland has an exciting opportunity for a REACH Toxicologist to join our Ashland Ingredients business at our Mumbai, India office. This is a very visible, significant role within the Company and the R&D function. This position will report to Sr. Manager Regulatory Affairs EMEA. The responsibilities of the position include, but are not limited to, the following: REACH (Registration, Authorizations, Restriction and Evaluation) compliance Gather and evaluate data for substances to be registered, identify data gaps and conduct read across assessments. Initiate and coordinate testing, or activities needed to address data gaps. Develop Exposure Scenarios for substances to be registered. Strategize to complete the Registration Dossier and submit to ECHA in a timely fashion, so that commercial REACH compliance needs are met. Update and carry out maintenance for continued compliance of already registered substances. Support responses to REACH questions from R&D, customers and commercial teams. REACH Support Provide support for analysis of REACH restricted substances and Substances of Very High Concern (SVHCs), including safety assessments of viable alternatives for Ashland’s raw materials and products. Support the provision of exposure scenario annexes for extended safety data sheets. Represent and defend Ashland’s position in REACH registration consortia meetings. Manage REACH data sharing activities Toxicology Consultation Provide support for hazard assessments of key chemicals. Conduct risk assessments for end uses. Provide written expert opinions. Provide technical support for toxicology-related R&D, commercial and customer responses. Develop and manage appropriate toxicological testing strategies; and support the coordination of non-REACH related testing. External Representation Represent Ashland at and participate in selected industry (e.g. cefic) and/or technical associations. Participate in professional development to stay current and up to date with the quickly evolving regulatory and toxicology landscape. Chemicals Management Support for Chemicals Management team as required on regulatory compliance activities related to chemicals regulations (EU REACH and CLP, UK REACH, ChemO (CH), KKDIK and SEA (TR), etc.) Regulatory Affairs The position will also include from time-to-time ad hoc regulatory compliance and project support for all Ashland business units (Life Sciences, Personal Care, Specialty Additives) in the EMEA region. In order to be qualified for this role, you must possess the following: Training in toxicology, industrial hygiene or chemistry desired with an overall 10 yr - 12 years of experience and a minimum 5 years of relevant REACH experience ( especially REACH registration) within the chemical industry. Experience in the use of exposure assessment tools (such as ConsExpo, ECETOC TRA, ART, Stoffenmanager, BEAT etc). Experience in the preparation of safety assessments and expert reports for regulatory (REACH) Registration/Dossier Submissions, using tools like CHESAR for chemical safety assessments (CSAs) and chemical safety reports (CSRs). Experience in conducting data gap analyses and devising testing strategies to assess the safety of chemicals to human and environmental health. Experience with QSAR is highly desirable. Experience with SAP EHS module is a plus. Language skills: fluent in English and proficiency in at least one other European language is a plus. Fast learner with a flexible style and the ability to adjust to changing business priorities. Highly accountable: solution-, results- and action-oriented. Results driven and highly responsive Out of the box, innovative thinking Excellent verbal / written communication and interpersonal skills. Ability to interface with internal and external contacts at all levels. Excellent organizational and prioritization skills. Ability to build teams and work collaboratively with peers Self-starter with ability to think and act independently and to make sound recommendations and decisions. Good analytical and problem-solving skills. Willingness to travel In more than 100 countries, the people of Ashland LLC. (NYSE: ASH) provide the specialty chemicals, technologies and insights to help customers create new and improved products for today and sustainable solutions for tomorrow. Our chemistry is at work every day in a wide variety of markets and applications, including architectural coatings, automotive, construction, energy, personal care and pharmaceutical. Visit www.ashland.com to see the innovations we offer. At Ashland our vision is to be a leading, global specialty chemicals company whose inspired and engaged employees add value to all we touch. In fact our people, employees, customers and vendors define who we are. They are the driving force behind everything we do. Not only do we value our customers but we value our employees, and we work to offer them a dynamic and challenging environment. We hold ourselves to high standards at Ashland, and we value integrity and honesty. Ashland has a history of attracting the best people and keeping them. The reasons are simple: industry competitive salary and benefits, pay-for-performance incentive plans and a diverse work environment where employees feel challenged and valued. People come to Ashland and stay. As a growing Fortune 500 specialty chemicals company, we offer opportunities for development and advancement throughout our global organization. Our values define who we are and what we care about as a company. If you are looking for a relationship with a company instead of simply a job, this may be a great fit. Ashland is proud to be an Equal Opportunity Employer Minorities/Women/Veterans/Disabled/Gender Identity/Sexual Orientation. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, or protected veteran status and will not be discriminated against on the basis of disability. NOTE: We do not accept resumes from external staffing agencies or independent recruiters for any of our openings unless we have a signed recruiting agreement in place to fill a specific position.

Kenvue is currently recruiting for a: Principal Scientist What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. Role reports to: 总监,毒理 Location: Asia Pacific, India, Maharashtra, Greater Mumbai Work Location: Fully Onsite What you will do Kenvue is currently recruiting for: Principle Scientist-Toxicology & Clinical Safety (skin tolerance) Who we are At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including Neutrogena, Aveeno, Tylenol, Listerine, Johnson’s and BAND-AID® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse and brilliant people, passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact the life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. Location : Mumbai What you will do Kenvue has products in beauty, baby, oral care, topical healthcare, personal hygiene and OTC franchises. Toxicology Resource Centre is engaged in the conduct of safety assessment of ingredients and products. This position entails conducting toxicology risk assessments for ingredients, finished products, impurities, and degradants, as well as evaluating topical skin safety for consumer products through data research and interpretation. It does not involve any laboratory work. Additionally, the role requires monitoring studies at Contract Research Organizations (CROs). Candidates should possess qualifications in Toxicology or Clinical Safety, along with experience in conducting in vitro or in vivo toxicology studies and/or skin tolerance studies, as well as risk assessment and medical writing skills. Responsibilities also include coordinating with third-party contractors, reviewing activities and assessments, mentoring junior scientists, and representing the team in technical and strategic discussions. Strong communication skills are essential for successful job performance. Job Responsibilities: Literature search and scientific data collection for preparation of hazard assessment report of the cosmetic ingredients Assessment of ingredients/raw materials/formulae at different stages of product development in skin care, essential health franchise Preparation of APR statements/Tox clearance statements and other relevant documents such as CPSRs, CCDS to support regional regulatory requirements as and when required Safety assessment of fragrances and flavors used in consumer products Preparation/Updating of INCI tox profiles The Principal Scientist (Toxicology/Clinical Safety) represents toxicology/safety in essential health and/or skin care franchise project teams and works with cross-functional business partners, PD team, RMC, the formulators, and suppliers etc. on a regular basis for obtaining more details regarding RMs, fragrances, formulas etc. to establish their pre-clinical safety strategies and perform their timely safety assessments in support of project timelines. Review of Assessment reports prepared by other Scientists and their approvals Representing AP tox team to attend global strategic discussion meeting on clinical safety Representing AP tox team to attend TRC discussion meeting. Mentoring junior scientist What we are looking for Master’s degree/ Ph.D. in toxicology, pharmacology or relevant science discipline. >3 years of experience in the field of consumer product risk assessment or other relevant Toxicology and/or Clinical safety (skin tolerance) experience. Diplomate of the American Board of Toxicology (DABT) certification, Diploma in clinical sciences preferred. In silico predictions Good verbal and written communication skill in English is a must. Individual with strong interpersonal skills and able to work independently Desirable: Knowledge of regulatory requirements for product safety submissions and experience in medical writing. What’s in it for you Competitive Benefit Package* Paid Company Holidays, Paid Vacation, Volunteer Time & More! Learning & Development Opportunities Employee Resource Groups This list could vary based on location/region Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process. Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

. Role Summary: Primary function will be to cost-effectively prepare regulatory-compliant Safety Data Sheet (SDS) documents for international customers who are outsourcing this function to the Managed Regulatory Services. Roles and Responsibilities: Effectively author regulatory compliant SDS/Labels for external customers for US, EU, CA and other countries. Search various reference sources and supplier SDS for required information and apply techniques to reconcile discrepancies in the sources. Perform evaluations according to toxicological, environmental, chemical, and physical properties for the determination of hazards of substances and chemical products. Perform quality control and regulatory compliance reviews of SDS/Labels prepared by others team members. Assist in establishing the details of the SDS/Labels content to be delivered contractually. Provide related services such as regulatory training, performing compliance reviews, writing procedures, and providing consultation services. Required Education: Experience and Education required in one or more of the following areas: University degree in Science (Chemistry, Biology, Toxicology, Environment, Health & Safety, Industrial Hygiene) or Chemical Engineering. Masters preferred. Knowledge of at least two of the following: REACH, GHS, OSHA, WHMIS, IATA, IMDG, ADR, ADNR, TDG, DOT Requirements: Work experience from 1 to 5 years, or more. Experience in sciences: Biology/Chemistry applications, Health/Safety/ Environmental regulations and/or toxicology. Experience in product stewardship or regulatory affairs. Experiences as a user of EH&S related software. Consulting experience. Self-starting /motivated. Attentive to detail. Ability to work on multiple assignments. Expect completing deadlines for more than one contract to be common. Strong regulatory analytical skills and troubleshooting skills. Reliable and take pride in work. Excellent team worker. Good verbal communication skills. Good written skills for reporting, writing procedures and providing regulatory information. Strong work ethic and professionalism. Committed to occasionally working extra hours to meet critical deliverable dates. Sphera is proud to be an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all colleagues.

Responsibilities You’ll be working on various projects in the natural resource sector with a focus on water quality and other environmental data screening, data management and statistical analysis You’ll support project teams with preparing written and graphical material for reports and presentations You’ll collaborate with teams across the company, including aquatics, toxicology, geochemistry, and hydrology. Software experience in GoldSim, MIKE3D, CE-QUAL-W2 You’ll collaborate with multi-disciplinary teams to complete environmental impact assessments and monitoring programs Qualifications A university degree (preferably MSc or PhD in environmental science, environmental engineering or geochemistry) Strong interpersonal, written, and verbal communication skills Technical skills in water quality assessment and analysis Advanced skills in Microsoft Excel Experience using data management software such as PowerBI Experience with computer programming in Python, R, and VB is an asset Ability to multi-task, maintain flexibility, and work independently About Us WSP is one of the world's leading professional services consulting firms. We are dedicated to our local communities and propelled by international brainpower. We are technical experts and strategic advisors including engineers, technicians, scientists, architects, planners, surveyors and environmental specialists, as well as other design, program and construction management professionals. We design lasting solutions in the Transportation & Infrastructure, Property & Buildings, Earth & Environment, Power & Energy, Resources and Industry sectors, as well as offering strategic advisory services. Our talented people around the globe engineer projects that will help societies grow for lifetimes to come. With approximately 4,000 talented people across 3 locations (Noida, Bengaluru & Mumbai offices) in India and more than 73,000 globally , in 550 offices across 40 countries , we engineer projects that will help societies grow for lifetimes to come. At “WSP” we draw on the diverse skills and capabilities of our employees globally to compete for the most exciting and complex projects across the world and bring the same level of expertise to our local communities. We are proud to be an international collective of innovative thinkers who work on the most complex problems. Unified under one strong brand, we use our local expertise, international reach and global scale to prepare our cities and environments for the future, connect communities and help societies thrive in built and natural ecosystems. True to our guiding principles, our business is built on four cornerstones: Our People, Our Clients, Our Operational Excellence and Our Expertise. www.wsp.com We are Passionate people doing purposeful and sustainable work that helps shape our communities and the future. A collaborative team that thrives on challenges and unconventional thinking. A network of experts channeling our curiosity into creating solutions for complex issues. Inspired by diversity, driven by inclusion, we work with passion and purpose. Working with Us At WSP, you can access our global scale, contribute to landmark projects and connect with the brightest minds in your field to do the best work of your life. You can embrace your curiosity in a culture that celebrates new ideas and diverse perspectives. You can experience a world of opportunity and the chance to shape a career as unique as you. Our Hybrid Working Module With us, you can operate in a flexible, agile, yet structured work environment and follow a Hybrid Work Model. Maximize collaboration. Maintain product quality and cultural integrity. Balance community, collaboration, opportunity, productivity, and efficiency. Health, Safety and Wellbeing Our people are our greatest asset, and we prioritize a safe work environment. Health, safety, and wellbeing are integral to our culture, with each of us accountable for fostering a safe workplace through our “Making Health and Safety Personal” initiative. Our Zero Harm Vision drives us to reduce risks through innovative solutions, earning recognition for our global health and safety practices with the prestigious RoSPA Health and Safety Awards for six consecutive years. Inclusivity and Diversity WSP India is dedicated to fostering a sustainable and inclusive work environment where our greatest strength - Our People -feel valued, respected, and supported. We ensure an unbiased approach in hiring, promotion, and performance evaluation, regardless of age, gender identity, race, religion, sexual orientation, marital status, physical ability, education, social status, or cultural background. Imagine a better future for you and a better future for us all. Join our close-knit community of over 73,300 talented global professionals dedicated to making a positive impact. Together, we can make a difference in communities both near and far. With us, you can. Apply today. NOTICE TO THIRD PARTY AGENCIES: WSP does not accept unsolicited resumes from recruiters, employment agencies, or other staffing services. Unsolicited resumes include any resume or hiring document sent to WSP in the absence of a signed Service Agreement where WSP has expressly requested recruitment/staffing services specific to the position at hand. Any unsolicited resumes, including those submitted to hiring managers or other business leaders, will become the property of WSP and WSP will have the right to hire that candidate without reservation – no fee or other compensation will be owed or paid to the recruiter, employment agency, or other staffing service.

Responsibilities You’ll be working on various projects in the natural resource sector with a focus on water quality and other environmental data screening, data management and statistical analysis You’ll support project teams with preparing written and graphical material for reports and presentations You’ll collaborate with teams across the company, including aquatics, toxicology, geochemistry, and hydrology. Software experience in GoldSim, MIKE3D, CE-QUAL-W2 You’ll collaborate with multi-disciplinary teams to complete environmental impact assessments and monitoring programs Qualifications A university degree (preferably MSc or PhD in environmental science, environmental engineering or geochemistry) Strong interpersonal, written, and verbal communication skills Technical skills in water quality assessment and analysis Advanced skills in Microsoft Excel Experience using data management software such as PowerBI Experience with computer programming in Python, R, and VB is an asset Ability to multi-task, maintain flexibility, and work independently About Us WSP is one of the world's leading professional services consulting firms. We are dedicated to our local communities and propelled by international brainpower. We are technical experts and strategic advisors including engineers, technicians, scientists, architects, planners, surveyors and environmental specialists, as well as other design, program and construction management professionals. We design lasting solutions in the Transportation & Infrastructure, Property & Buildings, Earth & Environment, Power & Energy, Resources and Industry sectors, as well as offering strategic advisory services. Our talented people around the globe engineer projects that will help societies grow for lifetimes to come. With approximately 4,000 talented people across 3 locations (Noida, Bengaluru & Mumbai offices) in India and more than 73,000 globally , in 550 offices across 40 countries , we engineer projects that will help societies grow for lifetimes to come. At “WSP” we draw on the diverse skills and capabilities of our employees globally to compete for the most exciting and complex projects across the world and bring the same level of expertise to our local communities. We are proud to be an international collective of innovative thinkers who work on the most complex problems. Unified under one strong brand, we use our local expertise, international reach and global scale to prepare our cities and environments for the future, connect communities and help societies thrive in built and natural ecosystems. True to our guiding principles, our business is built on four cornerstones: Our People, Our Clients, Our Operational Excellence and Our Expertise. www.wsp.com We are Passionate people doing purposeful and sustainable work that helps shape our communities and the future. A collaborative team that thrives on challenges and unconventional thinking. A network of experts channeling our curiosity into creating solutions for complex issues. Inspired by diversity, driven by inclusion, we work with passion and purpose. Working with Us At WSP, you can access our global scale, contribute to landmark projects and connect with the brightest minds in your field to do the best work of your life. You can embrace your curiosity in a culture that celebrates new ideas and diverse perspectives. You can experience a world of opportunity and the chance to shape a career as unique as you. Our Hybrid Working Module With us, you can operate in a flexible, agile, yet structured work environment and follow a Hybrid Work Model. Maximize collaboration. Maintain product quality and cultural integrity. Balance community, collaboration, opportunity, productivity, and efficiency. Health, Safety and Wellbeing Our people are our greatest asset, and we prioritize a safe work environment. Health, safety, and wellbeing are integral to our culture, with each of us accountable for fostering a safe workplace through our “Making Health and Safety Personal” initiative. Our Zero Harm Vision drives us to reduce risks through innovative solutions, earning recognition for our global health and safety practices with the prestigious RoSPA Health and Safety Awards for six consecutive years. Inclusivity and Diversity WSP India is dedicated to fostering a sustainable and inclusive work environment where our greatest strength - Our People -feel valued, respected, and supported. We ensure an unbiased approach in hiring, promotion, and performance evaluation, regardless of age, gender identity, race, religion, sexual orientation, marital status, physical ability, education, social status, or cultural background. Imagine a better future for you and a better future for us all. Join our close-knit community of over 73,300 talented global professionals dedicated to making a positive impact. Together, we can make a difference in communities both near and far. With us, you can. Apply today. NOTICE TO THIRD PARTY AGENCIES: WSP does not accept unsolicited resumes from recruiters, employment agencies, or other staffing services. Unsolicited resumes include any resume or hiring document sent to WSP in the absence of a signed Service Agreement where WSP has expressly requested recruitment/staffing services specific to the position at hand. Any unsolicited resumes, including those submitted to hiring managers or other business leaders, will become the property of WSP and WSP will have the right to hire that candidate without reservation – no fee or other compensation will be owed or paid to the recruiter, employment agency, or other staffing service.

Responsibilities You’ll be working on various projects in the natural resource sector with a focus on water quality and other environmental data screening, data management and statistical analysis You’ll support project teams with preparing written and graphical material for reports and presentations You’ll collaborate with teams across the company, including aquatics, toxicology, geochemistry, and hydrology. Software experience in GoldSim, MIKE3D, CE-QUAL-W2 You’ll collaborate with multi-disciplinary teams to complete environmental impact assessments and monitoring programs Qualifications A university degree (preferably MSc or PhD in environmental science, environmental engineering or geochemistry) Strong interpersonal, written, and verbal communication skills Technical skills in water quality assessment and analysis Advanced skills in Microsoft Excel Experience using data management software such as PowerBI Experience with computer programming in Python, R, and VB is an asset Ability to multi-task, maintain flexibility, and work independently About Us WSP is one of the world's leading professional services consulting firms. We are dedicated to our local communities and propelled by international brainpower. We are technical experts and strategic advisors including engineers, technicians, scientists, architects, planners, surveyors and environmental specialists, as well as other design, program and construction management professionals. We design lasting solutions in the Transportation & Infrastructure, Property & Buildings, Earth & Environment, Power & Energy, Resources and Industry sectors, as well as offering strategic advisory services. Our talented people around the globe engineer projects that will help societies grow for lifetimes to come. With approximately 4,000 talented people across 3 locations (Noida, Bengaluru & Mumbai offices) in India and more than 73,000 globally , in 550 offices across 40 countries , we engineer projects that will help societies grow for lifetimes to come. At “WSP” we draw on the diverse skills and capabilities of our employees globally to compete for the most exciting and complex projects across the world and bring the same level of expertise to our local communities. We are proud to be an international collective of innovative thinkers who work on the most complex problems. Unified under one strong brand, we use our local expertise, international reach and global scale to prepare our cities and environments for the future, connect communities and help societies thrive in built and natural ecosystems. True to our guiding principles, our business is built on four cornerstones: Our People, Our Clients, Our Operational Excellence and Our Expertise. www.wsp.com We are Passionate people doing purposeful and sustainable work that helps shape our communities and the future. A collaborative team that thrives on challenges and unconventional thinking. A network of experts channeling our curiosity into creating solutions for complex issues. Inspired by diversity, driven by inclusion, we work with passion and purpose. Working with Us At WSP, you can access our global scale, contribute to landmark projects and connect with the brightest minds in your field to do the best work of your life. You can embrace your curiosity in a culture that celebrates new ideas and diverse perspectives. You can experience a world of opportunity and the chance to shape a career as unique as you. Our Hybrid Working Module With us, you can operate in a flexible, agile, yet structured work environment and follow a Hybrid Work Model. Maximize collaboration. Maintain product quality and cultural integrity. Balance community, collaboration, opportunity, productivity, and efficiency. Health, Safety and Wellbeing Our people are our greatest asset, and we prioritize a safe work environment. Health, safety, and wellbeing are integral to our culture, with each of us accountable for fostering a safe workplace through our “Making Health and Safety Personal” initiative. Our Zero Harm Vision drives us to reduce risks through innovative solutions, earning recognition for our global health and safety practices with the prestigious RoSPA Health and Safety Awards for six consecutive years. Inclusivity and Diversity WSP India is dedicated to fostering a sustainable and inclusive work environment where our greatest strength - Our People -feel valued, respected, and supported. We ensure an unbiased approach in hiring, promotion, and performance evaluation, regardless of age, gender identity, race, religion, sexual orientation, marital status, physical ability, education, social status, or cultural background. Imagine a better future for you and a better future for us all. Join our close-knit community of over 73,300 talented global professionals dedicated to making a positive impact. Together, we can make a difference in communities both near and far. With us, you can. Apply today. NOTICE TO THIRD PARTY AGENCIES: WSP does not accept unsolicited resumes from recruiters, employment agencies, or other staffing services. Unsolicited resumes include any resume or hiring document sent to WSP in the absence of a signed Service Agreement where WSP has expressly requested recruitment/staffing services specific to the position at hand. Any unsolicited resumes, including those submitted to hiring managers or other business leaders, will become the property of WSP and WSP will have the right to hire that candidate without reservation – no fee or other compensation will be owed or paid to the recruiter, employment agency, or other staffing service.

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 part of the Jubilant Pharmova family of companies with R and 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 pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology and In-vitro ADME Medicinal Chemistry Synthetic and Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world's leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com ;;;;; ; The Position Organization; : - Jubilant Biosys Designation and Level: - SRA Location: - Greater Noida Department: - Analytical Key Responsibilities Having exposure of 1-8y in analytical chemistry (SFC or purification) Interaction with synthetic team and problem solving skills. Should be able to handle the respective instrument Knowledge of instrumental technique with its application Should be able to handle routine analysis independently on respective instrument . SFC: Support analytical chiral method development, chiral purification in SFC/Normal Phase. Maintain TAT as per target. Periodic maintenance, calibration of SFC instruments, completing documentation on time, performing additional analysis (chiral screening) when required. Candidate requirements: . ;;;; Educational qualification: Post Graduate Degree in Chemical/Life Sciences - M. Pharm, M. Sc., . ;;;; Technical Knowledge: ; Person Profile Qualification: - M. Sc (Analytical Chemistry) Experience: - 2 years of relevant experience Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

Job description: Candidates within Karnataka can apply. Key Responsibilities Assist in in vivo and in vitro studies, including animal handling, dosing, observations, and sample collection (blood, tissues, urine, etc.). Support toxicology and pharmacology studies under GLP protocols and SOPs. Work in vivarium settings , ensuring ethical animal care and welfare standards. Operate lab instruments (e.g., HPLC, LC-MS, balances, centrifuges ) and assist in routine calibration and maintenance. Perform basic lab assays (ELISA, blood chemistry, histology prep). Document experimental data in compliance with GLP : raw data forms, lab notebooks, equipment logs, and checklists. Coordinate with Study Directors and QA for audits, inspections, and compliance. Maintain inventory of lab consumables and assist in ordering supplies. Participate in report drafting and data analysis under supervision. Required: B.Sc. / M.Sc. in Life Sciences, Biotechnology, Pharmacology, Zoology, Biochemistry, or related field. Basic understanding of GLP principles , laboratory safety, and SOP-driven work. Preferred: 0–2 years of experience in a preclinical CRO or academic research lab . Exposure to toxicology, pharmacology, or DMPK studies. Knowledge of animal handling and CPCSEA guidelines (for Indian CROs). Strong organizational and documentation skills. Job Type: Full-time Pay: ₹13,000.00 - ₹18,000.00 per month Work Location: In person

Salesman with a chemical background (BBSC) or interest Experience in sales mainly for the Maharashtra region. Main Office: Mumbai Parel Office: Home office 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. Diphoterine® is increasingly recognized as the most efficient solution to prevent chemical burns and avoid serious medical consequences after a chemical splash in manufacturing units. Present in over 48 countries, Diphoterine® is recommended by national health services in France, UK, and Germany in official guidelines. With a presence of over 15 years in India, our company has earned an outstanding reputation with occupational health practitioners and Safety engineers in over 1000 companies. Main website: www.prevor.com PREVOR in India: www.hsesolutions.in To further increase our presence in Indian industries facing chemical risks, we are looking for an experienced Salesman with a interest into safety products. As the company is fast growing in India, you must be independent, hardworking, and reliable. Many business trips are involved for sales in Chennai and South (on average at least 3-4 days per week) + team meetings in Mumbai every two weeks. You will receive training in two stages: firstly, to understand PREVOR solutions, and secondly, to master our sales, management, and decision-making methods. As a salesman, you would work closely with the sales manager based in Mumbai. Your responsibilities will then be: To develop PREVOR’s business : You will analyze and understand customers' problems and needs and propose the most appropriate solutions. With your hands-on experience, you'll be able to assess chemical risks on site, and position yourself as the natural contact for specifiers and opinion leaders in your sector. You'll become a real ambassador for our offer at trade shows, professional conventions, scientific seminars, etc. Industry: pharma & all industries using chemicals in their manufacturing processes Some customers: Pharma: Sunpharma, Lupin, Cipla, Teva, Ipca, Sandoz etc… Photovoltaic industry: Jupitar Solar, Adani etc Chemical: Reliance, Atul, Jubilant, SI Group, Lonsen Kiri, Aarti, Srf etc Fertilizers: RCF, Deepak fertilizers, UPL etc. Mining: Vedanta, Hindustan Zinc; Pre-requisites: Degree in chemistry (BSC) minimum Interest / experience in sales (>2 year), Good interaction skills with people Fluency in both oral and written English + Tamil or Telugu In return, high rewards, respect and internal promotion are to be expected. Salary: depending on experience + commissions on sales 3% of the new clients + targets Finally, our company ethics insists on punctuality, seriousness, and hard work. Starting date: Immediately A background check will be done by our recruitment team.

Candidates within Karnataka can apply. Key Responsibilities Assist in in vivo and in vitro studies, including animal handling, dosing, observations, and sample collection (blood, tissues, urine, etc.). Support toxicology and pharmacology studies under GLP protocols and SOPs. Work in vivarium settings , ensuring ethical animal care and welfare standards. Operate lab instruments (e.g., HPLC, LC-MS, balances, centrifuges ) and assist in routine calibration and maintenance. Perform basic lab assays (ELISA, blood chemistry, histology prep). Document experimental data in compliance with GLP : raw data forms, lab notebooks, equipment logs, and checklists. Coordinate with Study Directors and QA for audits, inspections, and compliance. Maintain inventory of lab consumables and assist in ordering supplies. Participate in report drafting and data analysis under supervision. Required: B.Sc. / M.Sc. in Life Sciences, Biotechnology, Pharmacology, Zoology, Biochemistry, or related field. Basic understanding of GLP principles , laboratory safety, and SOP-driven work. Preferred: 0–2 years of experience in a preclinical CRO or academic research lab . Exposure to toxicology, pharmacology, or DMPK studies. Knowledge of animal handling and CPCSEA guidelines (for Indian CROs). Strong organizational and documentation skills. Job Types: Full-time, Fresher Pay: ₹13,000.00 - ₹18,000.00 per month Expected Start Date: 10/09/2025

About us At ExxonMobil, our vision is to lead in energy innovations that advance modern living and a net-zero future. As one of the world s largest publicly traded energy and chemical companies, we are powered by a unique and diverse workforce fueled by the pride in what we do and what we stand for. The success of our Upstream, Product Solutions and Low Carbon Solutions businesses is the result of the talent, curiosity and drive of our people. They bring solutions every day to optimize our strategy in energy, chemicals, lubricants and lower-emissions technologies. We invite you to bring your ideas to ExxonMobil to help create sustainable solutions that improve quality of life and meet society s evolving needs. Learn more about our What and our Why and how we can work together . ExxonMobil s affiliates in India ExxonMobil s affiliates have offices in India in Bengaluru, Mumbai and the National Capital Region. ExxonMobil s affiliates in India supporting the Product Solutions business engage in the marketing, sales and distribution of performance as well as specialty products across chemicals and lubricants businesses. The India planning teams are also embedded with global business units for business planning and analytics. ExxonMobil s LNG affiliate in India supporting the upstream business provides consultant services for other ExxonMobil upstream affiliates and conducts LNG market-development activities. The Global Business Center - Technology Center provides a range of technical and business support services for ExxonMobil s operations around the globe. ExxonMobil strives to make a positive contribution to the communities where we operate and its affiliates support a range of education, health and community-building programs in India. Read more about our Corporate Responsibility Framework. To know more about ExxonMobil in India, visit ExxonMobil India and the Energy Factor India . What role you will play in our team The Global Hazard Communication Advisor is responsible for delivering Safety Data Sheets (SDS) and related Chemical Management information to support the ExxonMobil Product Safety Policy and regulatory compliance globally The Specialist covers related functions including SDS Authoring, applied toxicology for chemical classification, product stewardship and regulatory interpretation, and related information-management-system support The position works closely with Marketing, Technology, and Regulatory Advisors What you will do Plan and execute SDS and related projects in coordination with business teams and stakeholders Work within established processes to assemble information and publish SDS Assign exposure scenarios and risk management measures for EU-REACH extended SDS development Read and interpret Hazard Communication regulations to determine impacts on product classification and labelling Support business partners in assessing new or reformulated products for classification and labelling purposes Evaluate new chemical classifications and maintain current and accurate data for SDS development Support the Product Stewardship Information Management System functions and interfaces with other systems Utilize software tools to classify product hazards based on composition, physical and chemical properties, and applicable chemical control regulations Support EU REACH product safety dossier development and submission using various tools such as IUCLID Identify and promote continuous improvement opportunities in systems and procedures About You Skills and Qualification BE / B Tech (Chemical / Materials / Polymers / Petroleum) or Masters in Pharmacology, Chemistry, Engineering, or other science discipline with minimum CGPA 6.5 or 65% Minimum 1 years of experience in petrochemical laboratories, or experience in product stewardship, toxicology, or chemical safety function Experience in SDS Authoring is required REACH Regulations is must IT System and Product Stewardship data management experience strongly preferred Preferred Skills and Qualifications Understanding of physical and chemical properties such as density, viscosity, and flash point Familiarity with regulations for Chemical Classification and Labelling and Product Transportation Classification Strong English communication skills Familiarity with common software including MS Excel, Word, PowerPoint Self motivated with ability to work independently and with global teams Well organized with attention to detail and concern for accuracy Your benefits An ExxonMobil career is one designed to last. Our commitment to you runs deep: our employees grow personally and professionally, with benefits built on our core categories of health, security, finance and life. We offer you: Competitive compensation Medical plans, maternity leave and benefits, life, accidental death and dismemberment benefits Retirement benefits Global networking & cross-functional opportunities Annual vacations & holidays Day care assistance program Training and development program Tuition assistance program Workplace flexibility policy Relocation program Transportation facility Please note benefits may change from time to time without notice, subject to applicable laws. The benefits programs are based on the Company s eligibility guidelines. Stay connected with us Learn more about ExxonMobil in India, visit ExxonMobil India and Energy Factor India . Follow us on LinkedIn and Instagram Like us on Facebook Subscribe our channel at YouTube EEO Statement ExxonMobil is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin or disability status. Business solicitation and recruiting scams ExxonMobil does not use recruiting or placement agencies that charge candidates an advance fee of any kind (e.g., placement fees, immigration processing fees, etc.). Follow the LINK to understand more about recruitment scams in the name of ExxonMobil. Nothing herein is intended to override the corporate separateness of local entities. Working relationships discussed herein do not necessarily represent a reporting connection, but may reflect a functional guidance, stewardship, or service relationship. Exxon Mobil Corporation has numerous affiliates, many with names that include ExxonMobil, Exxon, Esso and Mobil. For convenience and simplicity, those terms and terms like corporation, company, our, we and its are sometimes used as abbreviated references to specific affiliates or affiliate groups. Abbreviated references describing global or regional operational organizations and global or regional business lines are also sometimes used for convenience and simplicity. Similarly, ExxonMobil has business relationships with thousands of customers, suppliers, governments, and others. For convenience and simplicity, words like venture, joint venture, partnership, co-venturer, and partner are used to indicate business relationships involving common activities and interests, and those words may not indicate precise legal relationships.

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 Customer Centricity, Accountability, Bias to Action, Innovation, and Collaboration. These values help us recruit the right talent to join our rapidly expanding team of around the globe. It is important to us that each and every Spherion is not only eager to challenge themselves and knows how to get work done but is an awesome addition to our company culture. Primary function will be to cost-effectively prepare regulatory-compliant Safety Data Sheet (SDS) documents for international customers who are outsourcing this function to the Managed Regulatory Services. Roles And Responsibilities Effectively author regulatory compliant SDS/Labels for external customers for US, EU, CA and other countries. Search various reference sources and supplier SDS for required information and apply techniques to reconcile discrepancies in the sources. Perform evaluations according to toxicological, environmental, chemical and physical properties for the determination of hazards of substances and chemical products. Perform quality control and regulatory compliance reviews of SDS/Labels prepared by others team members. Assist in establishing the details of the SDS/Labels content to be delivered contractually. Provide related services such as regulatory training, performing compliance reviews, writing procedures and providing consultation services. Required Education Experience and Education required in one or more of the following areas: University degree in Science (Chemistry, Biology, Toxicology, Environment, Health & Safety, Industrial Hygiene) or Chemical Engineering. Masters preferred. Knowledge Of At Least Two Of The Following REACH, GHS, OSHA, WHMIS, IATA, IMDG, ADR, ADNR, TDG, DOT Required Experience Work experience from 1 to 5 years, or more. Experience in sciences: Biology/Chemistry applications, Health/Safety/ Environmental regulations and/or toxicology Experience in product stewardship or regulatory affairs Experiences as a user of EH&S related software Consulting experience Skills Self-starting / motivated. Attentive to detail. Ability to work on multiple assignments. Expect completing deadlines for more than one contract to be common. Strong regulatory analytical skills and troubleshooting skills. Reliable and take pride in work. Excellent team worker. Good verbal communication skills. Good written skills for reporting, writing procedures and providing regulatory information. Strong work ethic and professionalism. Committed to occasionally working extra hours to meet critical deliverable dates.

-Teach forensic medicine, conduct research, and participate in medico-legal autopsies. MD in Forensic Medicine required. Strong research and teaching background.

Company Description Jai Research Foundation is a prominent organization based in Valsad, India, near the Next to Daman Ganga Bridge, N.H. No. 8 Valvada. Known for its excellence in scientific research, Jai Research Foundation provides advanced solutions in various domains. The foundation is committed to fostering innovation and upholding the highest standards in research and development activities. Role Description This is a full-time on-site role for a Study Director in DART (Developmental and Reproductive Toxicology) Studies, located in Vapi. The Study Director will be responsible for overseeing and managing DART studies, coordinating projects, and ensuring compliance with regulatory standards. Key tasks include designing and executing in vivo experiments, performing toxicological assessments, managing laboratory operations, and leading research initiatives. Qualifications Laboratory Skills and In Vivo techniques Research and Toxicology proficiency Strong Project Management capabilities Excellent interpersonal and communication skills Ability to work independently and collaboratively in a team-oriented environment PhD or Master's degree in Toxicology, Pharmacology, or a related field Experience in DART studies and familiarity with regulatory guidelines is highly desirable

Job Description Designing and implementing toxicology studies in compliance with Good Laboratory Practice (GLP) standards. Conducting toxicological assessments, including acute. Chronic, Reptox, and Carci toxicity studies. Analyzing and interpreting data from in vivo and in vitro toxicology studies. Collaborating with multidisciplinary teams to ensure the integration of toxicology findings into overall study outcomes. Preparing and reviewing toxicology sections for regulatory submissions. Ensuring compliance with GLP regulations and maintaining accurate records.

Job Description You’re not the person who will settle for just any role. Neither are we. Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference. Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands. In this role, you’ll help us deliver better care for billions of people around the world. It starts with YOU. In This Role, You Will Represents the Global Product Safety, Stewardship, and Medical Affairs teams and works closely with cross-functional partners in product development, quality and regulatory affairs, to coordinate the development and execution of plans and deliverables within necessary timelines to ensure that all new and existing products meet or exceed both K-C requirements and regulatory/legal requirements. You will responsible for maintaining enterprise product stewardship programs to optimize business value by direction and guidance to the K-C business community to enable and meet product development milestones and ensure K-C products are safe for their intended use, support product registration/reporting as applicable, and comply with all applicable governmental safety and compliance rules, regulations, corporate standards, and consumer expectations through all phases of development, commercialization and post-market life cycle management. Represent the Product Safety, Stewardship and Medical Affairs teams with cross-functional partners to plan, manage, prioritize, and execute deliverables ensuring that all new and existing products meet or exceed both K-C requirements and safety/regulatory/legal requirements within necessary timelines. Perform technical activities in support material and product compliance, safety to human health, claims substantiation and stewardship programs through all phases of development, commercialization, and post-market life cycle management. Identify and escalate as appropriate technical or chemical compliance issues or material changes that may impact K-C products or business sectors. Conduct product and substance hazard classification, author and provide for hazard communication based on the Globally Harmonized System of Classification and Labeling of Chemicals (GHS) and local country requirements. As needed, coordinate product compliance testing to obtain necessary data for hazard classification, determination of compliance criterion, or registration or notification programs. Coordinate with business sectors to ensure ongoing compliance through change management, new product development and market expansion. Ensure data entered into SAP EHS for products and their materials are maintained with high quality standards in accordance with data models developed to support product safety, stewardship, and chemical regulation compliance. Support accurate product safety record documentation in SAP EHS database and manage chemical and ingredient regulatory compliance data and SAP reporting activities. Perform technical evaluations/assessments of products and their ingredients/raw materials sold in region to enable compliance to applicable standards and regulations. Communicate and support compliance actions. Identify and escalate as appropriate technical or chemical compliance issues or material changes that may impact K-C products or business sectors. Review product hazard classifications and Safety Data Sheets (SDSs) based on the Globally Harmonized System of Classification and Labeling of Chemicals (GHS) and local country requirements for accuracy and regional compliance. Designate and obtain necessary analytical test data as needed for hazard classification, determination of compliance criterion, or as needed for registration or notification programs. As needed, coordinate product compliance testing, including scheduling, test article shipment and final report review. Prepare chemical reporting data, ingredient listings and technical chemical compliance assessments for sustainability reporting, customer requirements and Regulatory Affairs in order meet regulatory obligations and product compliance determinations. Contribute to content for regulatory/chemical submissions in accordance with domestic local and regional regulatory requirements to support product development activities. Evaluate, appropriately process, and respond to incoming requests for chemical compliance information by applying technical knowledge of K-C products and regulations. Identify and escalate as appropriate technical or chemical compliance issues or material changes that may impact K-C products or business sectors. Build and develop relationships with internal and external business stakeholders including proactive participation in discussions with suppliers, external advisors and trade association(s) working groups. Evaluate, appropriately process, and respond to customer/consumer queries and questionnaires for chemical compliance/ stewardship by applying technical knowledge of K-C products and regulations to ensure compliance and support business growth. Provide support for Product Stewardship programs to ensure responsible stewardship and compliance of the regional K-C product portfolio. Capable to develop as a Subject Matter Expert (SME) in key areas of need, including regulatory compliance, toxicology and safety assessment, project management or systems development and maintenance. About Us Huggies®. Kleenex®. Cottonelle®. Scott®. Kotex®. Poise®. Depend®. Kimberly-Clark Professional®. You already know our legendary brands—and so does the rest of the world. In fact, millions of people use Kimberly-Clark products every day. We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you. At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth and impact. We’re founded on more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity. It’s all here for you at Kimberly-Clark. Led by Purpose. Driven by You About You You perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development. You love what you do, especially when the work you do makes a difference. At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results. When you join our team, you’ll experience Flex That Works: flexible work arrangements that empower you to have purposeful time in the office and partner with your leader to make flexibility work for both you and the business. Key Qualifications And Experiences In one of our technical roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center. To succeed in this role, you will need the following qualifications: Degree in biology, chemistry, toxicology, pharmacology, biomedical or a related technical field with 1-2 years of experience IT literacy and demonstrated proficiency in working within SAP database environments and Microsoft programs (Outlook, Excel, Word, PowerPoint, Visio, Project, etc.). Project management background/skills and ability to prioritize work activities. Demonstrated ability to understand and follow complex scientific/technical research, protocols, and procedures and the ability to analyze and interpret scientific data using computerized systems and databases. Knowledge of stewardship principles relevant to consumer product companies, chemical national inventories, chemical regulations, sustainability reporting approaches and product chemical and ingredient safety regulations globally. Experience applying the Globally Harmonized System of Classification and Labeling of Chemicals (GHS) standard for the generation of Safety Data Sheets and labeling requirements. Interpersonal communication and technical writing skills with demonstrated proficiency in working effectively in a multidisciplinary team. Demonstrated ability to effectively communicate and independently manage multiple projects in a cross-functional corporate setting and the ability to effectively communicate in written or oral presentation formats. Knowledge of toxicology or hazard assessment approaches for safety assessments. To Be Considered Click the Apply button and complete the online application process. A member of our recruiting team will review your application and follow up if you seem like a great fit for this role. In the meantime, please check out the careers website. And finally, the fine print…. For Kimberly-Clark to grow and prosper, we must be an inclusive organization that applies the diverse experiences and passions of its team members to brands that make life better for people all around the world. We actively seek to build a workforce that reflects the experiences of our consumers. When you bring your original thinking to Kimberly-Clark, you fuel the continued success of our enterprise. We are a committed equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity, age, pregnancy, genetic information, citizenship status, or any other characteristic protected by law. The statements above are intended to describe the general nature and level of work performed by employees assigned to this classification. Statements are not intended to be construed as an exhaustive list of all duties, responsibilities and skills required for this position. Employment is subject to verification of pre-screening tests, which may include drug screening, background check, and DMV check. Primary Location Mumbai Corporate Office Additional Locations Worker Type Employee Worker Sub-Type Regular Time Type Full time

[{"Salary":"40k - 50k per month" , "Remote_Job":false , "Posting_Title":"Senior Resident forensic medicine Tiruvannamalai" , "Is_Locked":true , "City":"Tiruvannamalai" , "Industry":"Hospitality" , "Job_Description":" Senior Resident in Forensic Medicine Role Summary: The Senior Resident in Forensic Medicine is responsible for performing forensic autopsies, providing expert testimony in court, interpreting injury patterns, collaborating with law enforcement, and ensuring the accurate documentation and analysis of forensic evidence. The role involves advanced forensic analysis, legal documentation, and maintaining ethical practices within the field. Key Responsibilities: Autopsy Performance: Conduct detailed post-mortem examinations to determine the cause and manner of death (natural, accidental, suicidal, or homicidal). Document findings, prepare autopsy reports, and ensure accurate record-keeping. Forensic Toxicology: Analyze biological samples (blood, urine, tissue) to detect toxins, drugs, alcohol, and poisons. Interpret toxicological results to assist in determining the cause of death or contributing factors. Injury Interpretation: Evaluate and interpret physical injuries from trauma, including blunt force, sharp force, gunshot wounds, and burns. Correlate injury patterns with possible causes, including criminal activity, accidents, or suicides. Legal Report Writing: Prepare comprehensive and legally sound reports summarizing post-mortem examination results. Ensure all reports meet legal standards for admissibility in court. Testifying in Court: Serve as an expert witness in court, providing clear, professional, and understandable testimony based on forensic findings. Respond to cross-examination and ensure objectivity in presenting evidence. Death Scene Investigation: Collaborate with law enforcement to investigate death scenes, assess evidence, and make preliminary determinations on the cause and manner of death. Provide expert advice on collecting and preserving physical evidence at the scene. Evidence Collection and Preservation: Ensure proper handling, storage, and chain of custody for forensic evidence, including biological samples and physical items from the crime scene. Maintain integrity of the evidence for laboratory analysis and court proceedings. Understanding of Legal Systems: Provide guidance on how forensic findings are integrated into legal procedures and support law enforcement investigations. Work closely with police, lawyers, and other legal professionals to ensure forensic evidence is used appropriately in the judicial process. Ethical Decision-Making: Uphold medical ethics, maintaining professionalism and confidentiality, especially in sensitive and high-stakes cases. Navigate complex ethical situations while balancing medical obligations and legal requirements. Crisis and Stress Management: Handle stressful and emotionally challenging situations, including traumatic cases, with composure and professionalism. Manage high-pressure environments, especially when dealing with time-sensitive or difficult forensic cases. Requirements Qualifications and Skills: Medical degree (MBBS or equivalent) with specialized training in Forensic Medicine. Experience in conducting autopsies and interpreting forensic evidence. Expertise in forensic toxicology, injury analysis, and death scene investigation. Strong written and verbal communication skills for report writing and court testimony. Understanding of forensic law and legal procedures related to medical evidence. Ability to handle high-stress situations and provide expert guidance in critical cases. Preferred Qualifications: Board certification or equivalent in Forensic Medicine. Experience in teaching or mentoring junior residents or medical students. Benefits 1. **Career Growth:*Opens doors to higher positions like Assistant Professor or Forensic Expert. 2. **Expertise Development:*Provides hands-on experience in autopsies, toxicology, and crime scene analysis. 3. **Job Security:*High demand in government hospitals, forensic labs, and law enforcement agencies. 4. **Legal Judicial Exposure:*Work closely with police, courts, and investigative bodies. 5. **Research Publications:*Opportunities to contribute to forensic research and academic papers. 6. **Higher Studies Specialization:*Pathway to pursue fellowships, PhD, or advanced forensic courses. 7. **Stable Income Benefits:*Government jobs offer good salaries, pensions, and additional perks. 8. **Networking:*Build connections with legal, medical, and law enforcement professionals. 9. **Public Service Impact:*Play a key role in delivering justice through medico-legal evidence. 10. **Teaching Opportunities:*Eligible for faculty roles in medical colleges and training institutes. ","Work_Experience":"3-5 years","Job_Type":"Full time" , "Job_Opening_Name":"Senior Resident forensic medicine Tiruvannamalai","State":"Tamil Nadu" , "Country":"India" , "Zip_Code":"606601" , "id":"14164000032942211" , "Publish":false , "Date_Opened":"2025-03-27" , "Keep_on_Career_Site":true}]