214 Toxicology Jobs - Page 7

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&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 &In-vitroADME Medicinal Chemistry Synthetic & 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 & Level: - Research Scientist/Sr. Research Scientist (L1/L2) Location : - Greater Noida Department: - Synthesis Reporting Manager: - Group Leader Key Responsibilities Synthesis, purification, and characterization of chemistry intermediates. Ability to lead 3-8 chemists. Deliver small to large quantities of lead novel chemical entities for drug discovery. Work collaboratively in a team to drive chemistry projects forward. Responsible for safe laboratory practices. Excellent knowledge of basic and advance organic chemistry. Very good knowledge of functional group conversion and multiple step synthesis. Knowledge of retrosynthetic analysis and route-designing of project. Good team leading skills of 3-8 chemists along with own-reactions. Excellent problem solving ability. Good expertise in handling various pyrophoric reactions and trouble-shooting. Good Knowledge of chiral chemistry, diastereomer separation. Excellent trouble-shooting skills in purification and extraction. Good Knowledge of (Prep)-HPLC and analyzing NMR, IR, Mass Spectrometry data. Excellent knowledge of writing and reviewing electronic lab notebooks; and writing reports, patents and manuscripts. Expertise in literature search using Reaxys/Scifinder etc. Always adhere to safe laboratory practices. Multi-tasking i.e. good in chemical ordering and maintaining lab inventory. Enthusiasm to create a dynamic research environment. Always stretch when project challenge increases. Excellent communication and presentation skill. Attention to the details. Ability to motivate team to work. Person Profile Qualification: - Ph.D in Organic Chemistry or related field /Post Doctorate Experience: - 1-5 years of industry/post-doc experiences. 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. Show more Show less

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 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 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 &In-vitroADME Medicinal Chemistry Synthetic & 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 & Level: - Research Associate -1/ Research Associate -2 (S1/S2) Location : - Greater Noida Department: - Synthesis Reporting Manager: - Group Leader Key Responsibilities 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 research environment. Always stretch when project challenge increases. Good knowledge in computer (MS-word/Excel/Power point) and structure drawing (Chem Draw/ISIS) and recording in electronic lab notebook. Good communication and presentation skill. Good in literature search using Reaxys. Person Profile Qualification: - M.Sc in Organic Chemistry or related field/ M. Pharma. Experience:- (below are Sample points) 1-6 years of industry experiences with any leading CRO organization. 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. Show more Show less

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 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 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 &In-vitroADME Medicinal Chemistry Synthetic & 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 & Level: - Research Associate -1/ Research Associate -2 (S1/S2) Location : - Greater Noida Department: - Synthesis Reporting Manager: - Group Leader Key Responsibilities 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 research environment. Always stretch when project challenge increases. Good knowledge in computer (MS-word/Excel/Power point) and structure drawing (Chem Draw/ISIS) and recording in electronic lab notebook. Good communication and presentation skill. Good in literature search using Reaxys. Person Profile Qualification: - M.Sc in Organic Chemistry or related field/ M. Pharma. Experience:- (below are Sample points) 1-6 years of industry experiences with any leading CRO organization. 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. Show more Show less

Assistant Professor 0-1 4 Raipur, 493661 Job Description Requirement Details Basic Qualification MBBS from a recognized institution Postgraduate Degree MD in Forensic Medicine from an NMC-recognized medical college Core Teaching Responsibilities Deliver undergraduate teaching in: Medical Jurisprudence Forensic Pathology Clinical Toxicology Ethics & Law in Medicine Assist in: Conducting practical sessions , including mock courts and forensic specimen demonstrations. Evaluating students through internal assessments and university exams. Preparing study material, question banks, and MCQs in alignment with CBME norms. ️ Practical & Legal Involvement Assist in medicolegal autopsies under the supervision of senior faculty. Support preparation of medicolegal reports including: Injury documentation Age estimation Cause of death Participate in: Hospital and police liaison for medicolegal cases Court appearances as expert witness (under mentorship) Research & Academic Development Collaborate in departmental and institutional research. Assist in: Literature reviews Data collection & analysis Drafting abstracts, papers, and case reports Attend: CMEs, conferences, faculty development programs (FDPs) Workshops in forensic science and medical education ️ Administrative & Support Duties Support Head of Department in: Curriculum planning Maintaining teaching schedules and student attendance records Help organize: Guest lectures Student activities (e.g., forensic quiz, debates) Departmental inspections and NMC documentation ✅ Desirable Attributes Confidence in communicating medico-legal concepts to students and non-medical stakeholders (e.g., police, legal teams). Basic familiarity with legal procedures , IPC/CrPC sections, and documentation standards. Skilled in dissection and forensic photography (advantageous). Comfort with digital teaching tools and virtual learning platforms Full Time 2200k Year Forensic Medicine And Toxicology Contact us For more information, contact us on admin@vitalityhealthcare.in

Associate Professor 4 1 Raipur, 493661 Job Description 1. Academic Qualifications: MBBS degree from a recognized medical college/institution. MD (Forensic Medicine) from an NMC-recognized institution. 2. Teaching & Experience Requirements: Minimum of 4 years teaching experience as an Assistant Professor in the subject (Forensic Medicine & Toxicology) in a recognized medical college. 3. Research Publications: Must have at least 2 research publications in indexed/national/international journals during the tenure as Assistant Professor. Key Responsibilities of Associate Professor in FMT A. Teaching & Academics Teach MBBS students forensic medicine, medical jurisprudence, clinical toxicology, and medico-legal aspects. Conduct practical classes , including autopsy demonstrations, mock court trials, and toxicology lab training. Supervise preparation of students for internal and university examinations. B. Research and Publications Conduct research in forensic science and clinical/applied toxicology. Guide junior faculty and students in research methodology and publications. Publish findings in reputable journals to contribute to departmental academic strength. C. Medicolegal & Administrative Duties Participate in medicolegal autopsies , injury assessments, age estimations, and court-related duties (appear as expert witness, etc.). Maintain records and reports as per institutional and legal standards. Assist the HoD in managing the department and planning academic activities. D. Curriculum and Faculty Development Participate in curriculum development (especially CBME – Competency-Based Medical Education). Attend and contribute to CME programs, faculty development programs, workshops, and departmental meetings. Full Time 3600k Year Forensic Medicine And Toxicology Contact us For more information, contact us on admin@vitalityhealthcare.in

Professor 7+ 1 Raipur, 493661 Job Description 1. Academic Qualifications: MBBS degree from a recognized institution. MD (Forensic Medicine) from an institution recognized by NMC. 2. Teaching & Experience Requirements: A total of 8 years of teaching experience in the subject (Forensic Medicine) as a Lecturer/Assistant Professor or equivalent, with at least 5 years as Associate Professor in a recognized medical college. Job Responsibilities of a Professor in FMT: Teaching MBBS and postgraduate students (if applicable) in Forensic Medicine. Supervising medicolegal autopsies and toxicology lab work. Conducting and guiding research in forensic science and toxicology. Managing departmental administration and academic planning. Preparing students for examinations and evaluating their academic performance. Coordinating with law enforcement and judiciary in legal cases requiring medical expertise. Full Time 4000k Year Forensic Medicine And Toxicology Contact us For more information, contact us on admin@vitalityhealthcare.in

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 Poland, Warsaw site. 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: 1. REACH (Registration, Authorisation, 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. 2. 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 3. 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. 4. 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. 5. 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.) 6. 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 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.

Job Advertisement Advertisement Date: 14.05.2025 Amity University Uttar Pradesh, Noida invites applications for Amity Institute of Environmental Toxicology Safety and Management (AIETSM) for Junior Research Fellow (JRF) Name of Post Junior Research Fellow (JRF) Number of Post 01 (One) Name of Project Identification of bioactive non-ribosomal peptide molecules from bacterial isolates of Indian sector of Southern Ocean Name of Sponsoring Agency Ministry of Earth Sciences, Govt. of India (MoES) Duration of the Position 2 Years Fellowship / Monthly Compensation As per MoES norms Essential Qualifications M.Sc. in Microbiology / Microbial Biotechnology / Life Science/ Biotechnology / Bioinformatics / Environment Science / Applied Science / B.Tech-Biotechnology Desirable Qualifications NET/GATE would be preferred Age Limit 28 years Interested candidates meeting the above qualifications are requested to send their detailed CV within 15 days of this advertisement through email to [email address] with cc to [email address]. Please mention JRF- AIETSM in the subject line. No TA/ DA will be paid to the candidates for attending the interview. Show more Show less

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 with our customer administrative staff to clarify plan provisions and resolve claim discrepancies. Respond to written inquiries from policyholders, beneficiaries, attorneys and families of deceased employees. Provide guidance on claim processes and resolve customer issues swiftly and thoroughly. Actively pursue and follow up on open claims within specified timeframe. Manage and organize work to meet multiple deadlines and competing priorities to ensure department turnaround and customer satisfaction are met. Evaluate life claims to identify claim situations requiring referral to Senior Examiner. Maintain good rapport with internal and external customers by taking ownership and projecting an attitude of service. Maintain production and quality standards. Keep up to date on Group Life procedures by using the Institutional Life Claims Library and attending required training. Use Microsoft Word and Excel to obtain information required to evaluate the life claim. Provide high quality, timely service to policyholders, beneficiaries, attorneys, families of deceased employees and administration; resolve customer issues swiftly and thoroughly by offering recommendations and solutions. Handle outbound calls needed in regard to Group Life servicing. Handle customer escalations from Reviewers and solve customer problems via telephone using sound business judgment. Respond to telephone referrals submitted regarding claim issues, research the claim as necessary and provide a response to the customer. Process claims withing Payment authority Maintain production and quality standards. Utilize BIOS, GLIF Production, CDF, Calligo, EDCS, Groupfacts, WorkDesk, NetView and Accurint to update and maintain accurate data. Interpret policy provisions and manually adjudicate Group Life claims. Initiate investigations, employing both company and outside facilities to obtain information to determine validity of Group Life claims. (Such as autopsy reports, toxicology reports, accident reports, location of missing beneficiaries, medical reports, homicide investigations, etc.) Mentor new Claim Examiners on Group Life procedures and workflow. Provide UAT support for system enhancements. Update & maintain day to day Workforce Management Preparing, Reporting & Analyzing the scorecards of performance Rules-based Decision Making Customer Relationship Management Identify possible alternative solutions and select the most appropriate ones Extracting data from various sheets and preparing custom defined reports Review/generate reports to monitor performance. Monitor transactions on an ongoing basis and take corrective steps where necessary or make incremental improvements. Provide coaching and feedback to team members to enable them to improve their performance. Assist new hires such that they are productive on the floor in the shortest possible time frame. Handle customer, employee, and internal partner escalations. Client Interaction, where required at the level of supervisors. Ensure compliance with internal policies and procedures, external regulations, and information security standards. Ensure that all agents in their process know their goals and how they are linked to the Organization’s quality policy. Motivate team members, anticipate staffing needs, acquire talent for the future, and manage attrition. Provide coaching and feedback to team members to enable them to improve their performance to raise individual and organizational capabilities. Effectively manage research/resolution/follow-ups for closure of open items. Build relationship with Onshore Management to ensure a “one-team approach”. About MetLife Recognized on Fortune magazine's list of the 2024 "World's Most Admired Companies" and Fortune World’s 25 Best Workplaces™ for 2024, MetLife , through its subsidiaries and affiliates, is one of the world’s leading financial services companies; providing insurance, annuities, employee benefits and asset management to individual and institutional customers. With operations in more than 40 markets, we hold leading positions in the United States, Latin America, Asia, Europe, and the Middle East. Our purpose is simple - to help our colleagues, customers, communities, and the world at large create a more confident future. United by purpose and guided by empathy, we’re inspired to transform the next century in financial services. At MetLife, it’s #AllTogetherPossible . Join us! Show more Show less

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 with our customer administrative staff to clarify plan provisions and resolve claim discrepancies. Respond to written inquiries from policyholders, beneficiaries, attorneys and families of deceased employees. Provide guidance on claim processes and resolve customer issues swiftly and thoroughly. Actively pursue and follow up on open claims within specified timeframe. Manage and organize work to meet multiple deadlines and competing priorities to ensure department turnaround and customer satisfaction are met. Evaluate life claims to identify claim situations requiring referral to Senior Examiner. Maintain good rapport with internal and external customers by taking ownership and projecting an attitude of service. Maintain production and quality standards. Keep up to date on Group Life procedures by using the Institutional Life Claims Library and attending required training. Use Microsoft Word and Excel to obtain information required to evaluate the life claim. Provide high quality, timely service to policyholders, beneficiaries, attorneys, families of deceased employees and administration; resolve customer issues swiftly and thoroughly by offering recommendations and solutions. Handle outbound calls needed in regard to Group Life servicing. Handle customer escalations from Reviewers and solve customer problems via telephone using sound business judgment. Respond to telephone referrals submitted regarding claim issues, research the claim as necessary and provide a response to the customer. Process claims withing Payment authority Maintain production and quality standards. Utilize BIOS, GLIF Production, CDF, Calligo, EDCS, Groupfacts, WorkDesk, NetView and Accurint to update and maintain accurate data. Interpret policy provisions and manually adjudicate Group Life claims. Initiate investigations, employing both company and outside facilities to obtain information to determine validity of Group Life claims. (Such as autopsy reports, toxicology reports, accident reports, location of missing beneficiaries, medical reports, homicide investigations, etc.) Mentor new Claim Examiners on Group Life procedures and workflow. Provide UAT support for system enhancements. Update & maintain day to day Workforce Management Preparing, Reporting & Analyzing the scorecards of performance Rules-based Decision Making Customer Relationship Management Identify possible alternative solutions and select the most appropriate ones Extracting data from various sheets and preparing custom defined reports Review/generate reports to monitor performance. Monitor transactions on an ongoing basis and take corrective steps where necessary or make incremental improvements. Provide coaching and feedback to team members to enable them to improve their performance. Assist new hires such that they are productive on the floor in the shortest possible time frame. Handle customer, employee, and internal partner escalations. Client Interaction, where required at the level of supervisors. Ensure compliance with internal policies and procedures, external regulations, and information security standards. Ensure that all agents in their process know their goals and how they are linked to the Organization’s quality policy. Motivate team members, anticipate staffing needs, acquire talent for the future, and manage attrition. Provide coaching and feedback to team members to enable them to improve their performance to raise individual and organizational capabilities. Effectively manage research/resolution/follow-ups for closure of open items. Build relationship with Onshore Management to ensure a “one-team approach”. About MetLife Recognized on Fortune magazine's list of the 2024 "World's Most Admired Companies" and Fortune World’s 25 Best Workplaces™ for 2024, MetLife , through its subsidiaries and affiliates, is one of the world’s leading financial services companies; providing insurance, annuities, employee benefits and asset management to individual and institutional customers. With operations in more than 40 markets, we hold leading positions in the United States, Latin America, Asia, Europe, and the Middle East. Our purpose is simple - to help our colleagues, customers, communities, and the world at large create a more confident future. United by purpose and guided by empathy, we’re inspired to transform the next century in financial services. At MetLife, it’s #AllTogetherPossible . Join us! Show more Show less

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 with our customer administrative staff to clarify plan provisions and resolve claim discrepancies. Respond to written inquiries from policyholders, beneficiaries, attorneys and families of deceased employees. Provide guidance on claim processes and resolve customer issues swiftly and thoroughly. Actively pursue and follow up on open claims within specified timeframe. Manage and organize work to meet multiple deadlines and competing priorities to ensure department turnaround and customer satisfaction are met. Evaluate life claims to identify claim situations requiring referral to Senior Examiner. Maintain good rapport with internal and external customers by taking ownership and projecting an attitude of service. Maintain production and quality standards. Keep up to date on Group Life procedures by using the Institutional Life Claims Library and attending required training. Use Microsoft Word and Excel to obtain information required to evaluate the life claim. Provide high quality, timely service to policyholders, beneficiaries, attorneys, families of deceased employees and administration; resolve customer issues swiftly and thoroughly by offering recommendations and solutions. Handle outbound calls needed in regard to Group Life servicing. Handle customer escalations from Reviewers and solve customer problems via telephone using sound business judgment. Respond to telephone referrals submitted regarding claim issues, research the claim as necessary and provide a response to the customer. Process claims withing Payment authority Maintain production and quality standards. Utilize BIOS, GLIF Production, CDF, Calligo, EDCS, Groupfacts, WorkDesk, NetView and Accurint to update and maintain accurate data. Interpret policy provisions and manually adjudicate Group Life claims. Initiate investigations, employing both company and outside facilities to obtain information to determine validity of Group Life claims. (Such as autopsy reports, toxicology reports, accident reports, location of missing beneficiaries, medical reports, homicide investigations, etc.) Mentor new Claim Examiners on Group Life procedures and workflow. Provide UAT support for system enhancements. Update & maintain day to day Workforce Management Preparing, Reporting & Analyzing the scorecards of performance Rules-based Decision Making Customer Relationship Management Identify possible alternative solutions and select the most appropriate ones Extracting data from various sheets and preparing custom defined reports Review/generate reports to monitor performance. Monitor transactions on an ongoing basis and take corrective steps where necessary or make incremental improvements. Provide coaching and feedback to team members to enable them to improve their performance. Assist new hires such that they are productive on the floor in the shortest possible time frame. Handle customer, employee, and internal partner escalations. Client Interaction, where required at the level of supervisors. Ensure compliance with internal policies and procedures, external regulations, and information security standards. Ensure that all agents in their process know their goals and how they are linked to the Organization’s quality policy. Motivate team members, anticipate staffing needs, acquire talent for the future, and manage attrition. Provide coaching and feedback to team members to enable them to improve their performance to raise individual and organizational capabilities. Effectively manage research/resolution/follow-ups for closure of open items. Build relationship with Onshore Management to ensure a “one-team approach”. About MetLife Recognized on Fortune magazine's list of the 2024 "World's Most Admired Companies" and Fortune World’s 25 Best Workplaces™ for 2024, MetLife , through its subsidiaries and affiliates, is one of the world’s leading financial services companies; providing insurance, annuities, employee benefits and asset management to individual and institutional customers. With operations in more than 40 markets, we hold leading positions in the United States, Latin America, Asia, Europe, and the Middle East. Our purpose is simple - to help our colleagues, customers, communities, and the world at large create a more confident future. United by purpose and guided by empathy, we’re inspired to transform the next century in financial services. At MetLife, it’s #AllTogetherPossible . Join us! Show more Show less

Key Responsibilities Having exposure of 1-4 years in analytical chemistry, method development and analysis of regular samples on chromatographic instruments (LC-MS). Candidate should be well acquainted with the respective instrument and software. Maintenance, cleaning, documentation and calibration of analytical instruments. Demonstrate perseverance, team co-ordination and analytical approach at the work place. Should be flexible with working hours. Provide training to new joiners. Practice safe work habits including complying with all safety health and environmental rules and regulations Person Profile Qualification: - M. Sc. (Analytical Chemistry)/ M. Pharm or related field from reputed university/institute. Experience: - 1-4 years of relevant experience for Masters.

We are hiring!!!!! Qualification: M.Sc. in life-science (Biotechnology and Microbiology Preferred). Experience: - 1 to 3 years of experience in Pharmacology and Toxicology (In-Vitro) with OECD GLP , NABL (ISO/IEC 17025:2017). << >>> Job description: Responsible for Cytotoxicity and Genotoxicity studies and their maintenance. Validated AMES and Cytotoxicity assays for medical devices according to ISO standards, ensuring accuracy and reliability in toxicological testing methodologies To act as a Study Director for in vitro studies as per the requirements of OECD GLP principle and ISO 17025. Should have performed Invivo Micronucleus assay, Ames assay & Chromosomal aberration. Authored comprehensive Standard Operating Procedures (SOPs) for laboratory activities Skills: Assays: AMES- bacterial reverse mutation assay, In vitro and In vivo micronucleus test and biochemistry parameters In vitro and In vivo Chromosome aberration test, Local Lymph Node Assay, Cell Gene Mutation assay Primary Cell lines handled. << >>> Benefits: Large campus with leave facilities like Casual Leave, Privilege leave, Sick leave School/college fees deduction for employee's staff Yearly Annual Health Check Up Report. Gym facility Hostel and Canteen facility. Employee engagement activities, tours and training and much more. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹63,078.48 per month Benefits: Food provided Leave encashment Paid sick time Paid time off Schedule: Morning shift Work Location: In person

Roles & Responsibilities End to end request governance for raw material data management - On-time initiation (within 24h of request receipt), adherence to the standard turnaround time (TAT) for all requests Understand the objective of the request. If needed, seek clarification/project background/missing information for initiating the request Handling supplier communication effectively, highlighting delays in getting supplier information & on-time escalation Timely update & maintenance of the Global Request Tracker (GTR) - GTR must be utilized as the single global source of reference for the entire lifecycle of each request within RM data management Timely, effective and transparent communication with global stakeholders for all requests Technical expertise - High standard of technical understanding of regulatory requirements for raw materials within all categories of use (Cosmetics, OTC, Drugs, Food/Nutritional s etc.) Knowledge of toxicology & safety assessment related information for raw materials within all categories of use (Cosmetics, OTC, Drugs, Food/Nutritional s etc.). Maintain a strong collaboration with the Toxicology partners to learn & quickly adapt for information requirement from suppliers as per specific request needs Data varsity - right first-time information collection & validity of the high volumes of data incoming for all requests should be maintained Understand the end-to-end data connectivity across all systems & maintain high standard of data accuracy at the time of data entry in the systems Sustain an Ownership Mindset - Complete all requests, right-first time & on-time (within TAT) Ensure to meet the KPIs on quality & productivity consistently Soft skills required (must have) - Project/ Request management - Given the huge number of requests that flow in this project, efficiency in overall & individual request, time & task management is highly required Disciplined execution & ability to provide attention to detail - Should be fully focused and evaluate the information thoroughly and follow the process in disciplined way to ensure on time visibility to the stakeholders and flawless execution to meet the individual request timelines. Communication skills - Effective, timely and proactive communication with all internal & external (suppliers) stakeholders Problem solving - Understand the criticality of the problem & seek practical, time-bound solutions to overcome the challenge Critical thinking - Asking right questions, avoidance of redundant questions, steps, processes & learning from past experiences to extrapolate the lessons to other requests Sense of urgency & learning Agility - Understand the urgency and its impact to the business. Apply the learnings immediately in the ongoing and future projects/work. Agility & Resilience - ability to work under fast paced conditions, taking quick alignments for faster decision making

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 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 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-vitromodels 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 &In-vitroADME Medicinal Chemistry Synthetic & 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 & Level : - RA Location: - Greater Noida Department: - Analytical Key Responsibilities Having exposure of 1-4 years in analytical chemistry, method development and analysis of regular samples on chromatographic instruments (LC-MS). Candidate should be well acquainted with the respective instrument and software. Maintenance, cleaning, documentation and calibration of analytical instruments. Demonstrate perseverance, team co-ordination and analytical approach at the work place. Should be flexible with working hours. Provide training to new joiners. Practice safe work habits including complying with all safety health and environmental rules and regulations Person Profile Qualification: - M. Sc. (Analytical Chemistry)/ M. Pharm or related field from reputed university/institute. Experience: - 1-4 years of relevant experience for Masters. 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.

Company DescriptionKrish Biotech Research Private Limited (KBRPL) is a leading Contract Research Organization (CRO) based in Kalyani, West Bengal, India. The company specializes in toxicology, analytical chemistry, bioanalytical studies, and environmental testing. KBRPL’s 100,000 square-foot facility is equipped with state-of-the-art laboratories that adhere to international standards. The company is GLP certified, ensuring high-quality research processes, and holds ISO/IEC 17025 certification, which further certifies their competence in laboratory testing and calibration. KBRPL’s research outputs are globally recognized and accepted, including by regulatory authorities in the USA, Brazil, Australia, and the EU. Role DescriptionThis is a full-time on-site role for Senior Research Scientist (Chemistry and Toxicology) located in Kolkata. The Senior Research Scientist will be responsible for designing, conducting, and analyzing complex experiments in the fields of toxicology, analytical chemistry, and environmental testing. Day-to-day tasks include developing testing protocols, managing laboratory staff, ensuring compliance with GLP standards, preparing research reports, and presenting findings to stakeholders. The role also involves maintaining accurate records, troubleshooting technical issues, and staying updated with industry trends and regulatory requirements. QualificationsExperience in toxicology, analytical chemistry, and environmental testingProficiency in developing research protocols and experimental designsStrong laboratory management and staff supervision skillsKnowledge of GLP standards and regulatory complianceExcellent analytical and problem-solving skillsOutstanding written and verbal communication abilitiesPh.D. or Master's degree in Chemistry, Toxicology, Environmental Science, or a related fieldPrior experience in a GLP-certified laboratory is a plus

Company Description Welcome to ZES Bioscience Pvt. Ltd., a global hub for toxicology testing and safety assessment services located in Bhopal. Our CCSEA-certified research facility ensures compliance with international standards, specializing in preclinical toxicology, pharmacokinetics, and safety assessment for pharmaceutical and chemical industries. We have a skilled workforce dedicated to helping clients make informed pipeline decisions, shaping the future of healthcare with precision and quality. Role Description This is a full-time on-site role for a Graphic Designer at ZES Bioscience Pvt. Ltd. The Graphic Designer will be responsible for creating visual concepts, developing branding materials, designing logos, working on typography, and creating graphics to support the company's communication and marketing efforts. Qualifications Graphics and Graphic Design skillsLogo Design and Branding experienceTypography skillsCreative thinking and problem-solving abilitiesProficiency in Adobe Creative Suite (Photoshop, Illustrator, InDesign)Strong attention to detail and time-management skills.

Job portal All vacancies 163925 Professor of Veterinary Biomedicine Professor of Veterinary Biomedicine Department of Veterinary and Animal Sciences Faculty of Health and Medical Sciences University of Copenhagen The University seeks to appoint a professor to the Department of Veterinary and Animal Sciences to commence 1 December 2025 or as soon as possible thereafter. Information on the department can be found at: https://www.sund.ku.dk/. Job Description When considering applications for the professorship, the main emphasis will be on the applicant's ability to document a high level of original scientific work at an international level within the area of Veterinary Biomedicine. The professorship is part of Section of Biomedicine that encompasses the topics of experimental and clinical pharmacology and toxicology, laboratory animal science and welfare, veterinary and nutritional immunology, comparative pediatrics and bioinformatics and are the main responsible for the biomedicine track on the veterinary education. Studying interactions between exposure and response in complex biological systems is a central part of the biomedicine track and thus research, supervision and teaching in this area will constitute the main focus of the professorship. This includes developing, validating and monitoring in vivo disease- and PK/PD models - for example for testing a novel drug in an experimental animal exhibiting a specific disease phenotype – and evaluating the pharmacokinetic (PK), pharmacodynamic (PD) and toxicological properties of a given compound. A successful candidate to the professorship must have substantial experience with these areas and across animal species. A broad and expanding field, Veterinary Biomedicine engages several disciplines. Besides pharmacology and toxicology, these include veterinary pathology, physiology and laboratory animal sciences. In addition, methods to analyze effects and endpoints are continuously emerging, encompassing areas within digital image analysis, histopathology, molecular biology and bioinformatics. A successful candidate must be able to document experience in at least some of these areas and show the ability to collaborate with colleagues from related disciplines. The professorship is required to develop and consolidate the field of Veterinary Biomedicine. This is expected to involve network activities through collaborations (e.g. with the biomedical industry), and through research-based education at pre- and postgraduate levels. Specifically, the professor will be responsible for the Biomedicine track for veterinary master students. Teaching activities include planning the course and curriculum, developing teaching materials, conducting practical and theoretical exercises and assessing students at the exam. Supervisor experience of bachelor, master and PhD projects, and supervision or mentorship of junior academic employees, is a requirement. Documented experience in research group management and leadership must also be included. The Professor’s Responsibilities Will Primarily Consist Of Research, including publication/academic dissemination and acquisition of external fundingResearch-based teaching, including associated examination, at all academic levelsResearch leadership, including guidance and supervision of researchersObligation to share knowledge with the rest of society, including participation in public debateAcademic assessments and active engagement in other administrative duties and committees within the Department and UCPH Required Qualifications To be qualified for a professor position, you will be assessed according to these six overall criteria for recognising merit at the University of Copenhagen: Research, teaching, societal impact, organisational contribution, external funding, and leadership. Find information about each criterion. Furthermore, Each Applicant Must Be Able To Document Document a high degree of original academic production at an international level, including considerable contributions to the development of the academic disciplineExtensive experience and formal training in leading a research groupExtensive experience to obtain and manage external funding for researchManage research and other management functions, e.g. engage in the university’s external academic activities, as well as knowledge and technology transferProvide research-based teaching including documentation of formal pedagogical qualifications and a record of pre and post graduate research-based teaching, preferable within the field of Veterinary Biomedicine The professor is also required to possess good interpersonal and communicative skills. Terms of employment The position is a permanent position. The average weekly working hours are 37 hours per week. Salary and other terms and conditions of appointment are set in accordance with the Agreement between the Ministry of Taxation and AC (Danish Confederation of Professional Associations) or other relevant professional organisations. The position is covered by the Job Structure for Academic Staff at Universities 2020. Questions For further information, please contact Head of Section, Professor Jens Lykkesfeldt (jopl@sund.ku.dk). Foreign applicants may find the university’s International Staff Mobility useful. Application The application must be submitted in English and must include the following documents: Application (Including motivation for applying for this position (Maximum 2 pages))Curriculum vitae (Including information about external funding)Diplomas (Master’s, PhD and other relevant certificates)A complete list of publicationsResearch plan (3‐5 pages)Uploads of maximum 10 publications to be considered in the assessmentTeaching planTeaching portfolio (Guidelines) Application procedure After the expiry of the deadline for applications, the authorized recruitment manager selects applicants for assessment on the advice of the Appointments Committee. All applicants are then immediately notified whether their application has been passed for assessment. The Dean then appoints an expert assessment committee in order to make an assessment of the selected applicants for the specific post. Selected applicants are notified of the composition of the committee and each applicant has the opportunity to comment on the part of the assessment that relates to the applicant him/herself. You can read about the recruitment process at the university's Job Portal. Please note that the applicant will be contacted if the assessment committee requires further documentation. The applicant will be assessed according to the Ministerial Order no. 242 of 13 March 2012 on the Appointment of Academic Staff at Universities. The University of Copenhagen encourages all interested applicants to apply for this position. Please submit the application with the required attachments. Only online applications will be accepted. The closing date for applications is 23.59 p.m. CET, 18 May 2025. Interviews for this position are likely to be held on 20 October 2025. APPLY NOW Part of the International Alliance of Research Universities (IARU), and among Europe’s top-ranking universities, the University of Copenhagen promotes research and teaching of the highest international standard. Rich in tradition and modern in outlook, the University gives students and staff the opportunity to cultivate their talent in an ambitious and informal environment. An effective organisation – with good working conditions and a collaborative work culture – creates the ideal framework for a successful academic career. Contact Jens Lykkesfeldt E-mail: jopl@sund.ku.dk Info Application deadline: 18-05-2025 Employment start: 01-12-2025 Working hours: Full time Department/Location: Department of Veterinary and Animal Sciences " id="cookiefilter-placeholder-1"> Content not available due to cookie preferences You cannot see the content of this field because of your cookie preferences. Click here to change your cookie settings. Category: Marketing Search all vacancies

Job description Company Description Diligence Bio is a preclinical contract research organization located in Puducherry, the largest city in the Indian union territory of Puducherry. The facility specializes in testing agrochemicals, pharmaceutical products for the regulatory market. They conduct acute toxicity, genetic toxicity, and ecotoxicity testing in compliance with OECD GLP principles. Role Description This is a full-time on-site role for a Study Director - Chemistry at Diligence Bio. The Study Director - Chemistry will be responsible for conducting research and development activities, performing chemistry-related tasks, toxicology studies, and analytical chemistry. The role involves working on-site at the facility located in Puducherry. Qualifications Chemistry expertise Toxicology experience Proficiency in Analytical Chemistry Strong scientific knowledge and analytical skills Attention to detail and accuracy Excellent written and verbal communication skills Ability to work effectively in a team Experience in the contract research organization (CRO) industry is a plus Masters's degree or higher in Chemistry or related field. Please share your CV to hr@diligencebio.com Job Type: Full-time Pay: ₹20,000.00 - ₹60,000.00 per month Benefits: Food provided Leave encashment Paid sick time Provident Fund Supplemental Pay: Yearly bonus Ability to commute/relocate: Pondicherry, Puducherry: Reliably commute or planning to relocate before starting work (Preferred) Experience: total work: 3 years (Preferred) Work Location: In person

PhD in Toxicology, Risk Assessment Modelling or closely related discipline Or Masters with 5-10 years chemicals industry. 5+ years of experience in toxicology. Knowledge of toxicology studies (design/data generated) required for regulatory agencies. Required Candidate profile Strong English skills, including scientific reports/ hazard evaluations and position papers. Knowledge of global regulation & GLP requirements for human health. Exp., in managing toxicology studies.

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 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 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-vitromodels 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 &In-vitroADME Medicinal Chemistry Synthetic & 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 & Level: - SRA Function: - Purification Location: - Greater Noida Department: - Analytical Key Responsibilities Having exposure of 1-6 years in analytical chemistry, method development and purification of samples on chromatographic instruments (HPLC/Prep-HPLC/SFC/Prep-SFC). Candidate should be able to handle routine analysis independently on respective instrument and trouble-shooting of respective analytical instruments. Knowledge of instrumental technique/software with its application Should be able to handle routine analysis independently on respective instrument, Experience in method development on LCMS will be desirable but not necessary. Practice safe work habits including complying with all safety health and environmental rules and regulation. Person Profile Qualification: - M. Sc. (Analytical Chemistry)/ M. Pharm or related field from reputed university/institute. Experience: - 2-10 years of relevant experience for Masters (depending on level) 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.

Role & responsibilities Teaching UG and PG students, Supervising Ph.D. research, designing and delivering courses, conducting research and publishing findings, mentoring students, and participating in departmental and university activities. Preferred candidate profile Candidate Should be M.Sc./Ph.D. in forensic science with expertise in Forensic Chemistry and Toxicology. Perks and benefits

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.

Author compliant Safety Data Sheets for multiple geographies across the globe as per applicable hazard communication regulations Derive hazard classifications for substances and mixtures using various classification regulations including but not limited to GHS, CLP, & OSHA Hazard Communication Standard Ensure CLP Classifications used in Azelis SDS for customized substances/preparation are in alignment with the ones reported to ECHA by Azelis Efficiently address queries from internal stakeholders & coordinate with Process Lead/SHEQ Specialist for quick resolution for high priority requests Assist in responding to external customer inquiries related to product classification and labelling Assist to develop and maintain internal processes that supports core functions of Group SHEQ support Services Center Follow work instructions & checklist as defined for each process across domains to ensure validity & integrity of Master data management activities Engage in quality management activities and handle complaints/ non-conformities effectively Execute effective change management program for applicable processes as and when required due to regulatory updates or business requirements Ensure quality of information in data management system is maintained and strive to achieve zero non-conformity Support in Training Associates/Interns on regulatory & process knowledge Ensure activity records are maintained as per defined formats Qualification & Skills University Degree (Equivalent to master s degree) in Chemistry, Biology, Environmental Sciences, Toxicology, or a related scientific discipline 2-4 years of experience related to product stewardship, chemical regulations & hazard communication Functional knowledge of chemistry, toxicology, ecotoxicology, and risk assessment as it applies to hazard communication and regulatory information Knowledge of international transport regulations (UN-RTDG, ADR, DOT, IATA, IMDG) Detail oriented with good time and project management skills, with an ability to switch priorities when required Customer service mindset along with ability to interact with multiple stakeholders while meeting their expectations Strong written and verbal communication skills (English) and Proficiency in French or Spanish will be added advantage Excellent IT skills, including strong proficiency in MS Excel, Word & PowerPoint Awareness of QMS ISO 9001:2005, Six sigma process will be an added advantage Comfortable to work in fixed & rotational shift including night shifts

Follow work instructions & checklist as defined for each process across domains to ensure validity & integrity of Master data management activities Maintain data quality & integrity by ensuring information in data management systems are as per most current health, safety, environmental & regulatory information from Safety Data Sheet Efficiently address queries from internal stakeholders & coordinate with Process Lead/SHEQ Specialist for quick resolution for high priority requests Engage in quality management activities as and when assigned Support in Training Associates/Interns on regulatory & process knowledge Utilize statistical tools for analyzing records and preparation of reports as requested by management Execute effective change management program for applicable processes as and when required due to regulatory updates or business requirements Ensure quality of information in data management system is maintained and strive to achieve zero non-conformity Ensure activity records are maintained as per defined formats Senior Associates will be responsible for maintaining the data across three domain - SHEQ, Operations & Marketing SHEQ Validate regulatory documentation & information of products including but not limited to GHS classification, REACh compliance, Biocides, Trade controls, Market segment specific regulations like Pharmaceuticals, Food, Cosmetics etc Maintain data quality & integrity by ensuring information in data management systems are as per most current health, safety, environmental & regulatory information Contribute to improvement of the quality of the data extraction automation for Safety Data Sheet & Technical Data Sheet Support the continuous optimization of our global processes Follow-up with business colleagues & principals for completion of SHEQ information in PIM Operations Validate operational & logistic documentation & information of products including but not limited to packaging, transport regulations, dangerous goods classification, shelf life, storage conditions, warehouse related data Maintain data quality & integrity by ensuring information in data management systems are as per most current operations & logistics information Contribute to improvement of the quality of the data extraction automation for Safety Data Sheet & Technical Data Sheet Support the continuous optimization of our global processes Follow-up with business colleagues & principals for completion of Operational information in PIM Marketing Validate marketing documentation & information of products including but not limited to product description, product application & other key data points for customer portal Retrieve and upload documents linked to the products Maintenance of our documents ageing and anticipate new request to Principals for nearly expired documents Maintain data quality & integrity by ensuring information in data management systems are as per most current marketing information Contribute to improvement of the quality of the data extraction automation for Technical Data Sheet, Product specification & Product catalogue Support the continuous optimization of our global processes Follow-up with business colleagues & principals for completion of Marketing information in PIM Qualification & Skills University Degree (Equivalent to master s degree) in Chemistry, Biology, Environmental Sciences, Toxicology, or a related scientific discipline 2-4 years of experience related to product stewardship, chemical regulations & hazard communication Knowledge of international transport regulations (UN-RTDG, ADR, DOT, IATA, IMDG) Detail oriented with good time and project management skills, with an ability to switch priorities when required Customer service mindset along with ability to interact with multiple stakeholders while meeting their expectations Strong written and verbal communication skills (English) and Proficiency in French or Spanish will be added advantage Excellent IT skills, including strong proficiency in MS Excel, Word & PowerPoint Awareness of QMS ISO 9001:2005, Six sigma process will be an added advantage Comfortable to work in fixed & rotational shift including night shifts