250 Toxicology Jobs

Company Description Syngenta We are a leading, science-based agriculture company, empowering farmers to meet the demands of modern agriculture. Using cutting-edge innovation, we help farmers to grow resilient, healthy crops that can feed a growing global population, while promoting sustainable farming practices that protect and enhance our planet. Headquartered in Switzerland, we are a global agritech leader with more than 30,000 employees across over 90 countries. https://www.syngenta.com/company Job Description This role requires > 8 years of experience working in the areas of pesticide/agrochemical formulation development and able to work in the formulation lab. Lead the development of Crop Protection formulations To formulate, generate scientific / technical data using established systems, procedures, and protocols in an area of work delegated by the manager. Define the experimental programme that include the development of new pesticide formulations, procedures/standards. To interpret data in order to make contributions to decisions in the work programme content, procedures, or problem solution. Engages directly with other functions to co-ordinate delivery of project outputs (e.g. product biology, regulatory, procurement team, engineering team, packaging etc) with the support of a leader. Report on work, including recommendations to project team or sub-project team leader. Participate in regional and global technical / project teams Will represent the formulation development work/status at every developmental stage to global peer review team and adhere to project timelines. Accountabilities To plan, organise and carry out the work programmes at the laboratory, semi-technical, pilot plant or manufacturing scale to design novel pesticide formulation options in order to: Prove the suitability for progression through Stage C and D Evaluation and Development Provide Product Chemistry type and or supporting data, and Provide the formulation design input required to define the process equipment and quality assurance requirements to timescales and specifications agreed with the team or group leader. Ensure the quality of Evaluation and Development formulations by arranging for biological efficacy, toxicology, and hazard assessment studies to be carried out in other Functions. Provide advice and recommendations to allow appropriate selection of formulation manufacturing sites for individual products, together with the product design inputs required to define the process equipment and quality assurance requirements. To interpret and represent to project members external to the function, experimental data and report results and conclusions obtained both orally and in written form to allow cogent and timely Stage C and D project decisions, Regulatory submissions and accurate information archiving and transfer for future commercial manufacturing activities. To ensure that work by the job holder and subordinate staff comply with Syngenta standard operating procedures and statutory regulations (e.g. GLP or similar). To ensure that the jobholder and subordinate staff work safely and healthy with due care for others, so that compliance with Syngenta’s HSE Policy is achieved. To invest in personal and professional development and growth, undertaking, where appropriate, training and development activities and ensuring familiarity with new research and literature. Ensure maintaining complete confidentiality of all Syngenta intellectual property. Interact with the global formulation community in order to better solve common problems and to define improved processes Qualifications KNOWLEDGE EXPERIENCE and CAPABILITIES: Critical Knowledge And Experience Master’s degree in Pesticide/Agrochemical chemistry must/preferable from reputed universities with strong academic records and good communication skills with > 8 years of industrial experience in field of pesticide formulation development as a formulation development chemist preferred. Thorough knowledge of pesticides, pesticide formulation types and techniques required in formulation development. Sound understanding of agrochemical formulations / Coformulations / Fillers is a must Critical Technical, Professional, And Personal Capabilities Ability to efficiently build up laboratory works and experiments Ability to effectively participation in- and contribute to regional / global multi-functional teams Ability to deliver to agreed timelines Excellent operational, organisational, interpersonal and computer skills Sensitive to different cultural environments Self-motivating Critical Leadership Capabilities Communicative We deliver clear messages to our stakeholders We are keen to listen and learn Team Oriented We model commitment We support team process improvement We collaborate effectively across organisational and functional boundaries Results Oriented We focus on goal achievement We stay focused Customer Focused We seek to understand our customers We build collaborative relationships Trusted We demonstrate support for others Critical success factors and key challenges This role will involve taking a lead role in the development of new formulations by generating potential formulation options through the design of appropriate experimental work programs to thoroughly optimise and test these according to the formulation development process. This will include the analysis of experimental data in order to make inputs to the decisions on the direction of the work programmes within the project. The job holder will need to have experience of different formulation types as well as a full range of broader requirements in formulation development such as product application, manufacturing processes, etc. To deliver highest quality results in optimal time and maintain highest standards of HSE Additional Information Additional Information : People Are At The Heart Of What We Do Once a year Full body check Competitive insurance scheme Employee assistance program – to take care of your and your loved ones mental health Paid Vacation of 30days, 12 Paid Holidays, Maternity and Paternity Leave, compassionate leaves Education assistance – for your career growth People first culture translated into ‘Most Preferred place to work 2022-23 by Times group’ Note: Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. To learn more visit: www.syngenta.com and www.good-growth-plan Follow us on: Twitter & LinkedIn Twitter LinkedIn

Company Description Syngenta We are a leading, science-based agriculture company, empowering farmers to meet the demands of modern agriculture. Using cutting-edge innovation, we help farmers to grow resilient, healthy crops that can feed a growing global population, while promoting sustainable farming practices that protect and enhance our planet. Headquartered in Switzerland, we are a global agritech leader with more than 30,000 employees across over 90 countries. https://www.syngenta.com/company Job Description This role requires > 8 years of experience working in the areas of pesticide/agrochemical formulation development and able to work in the formulation lab. Lead the development of Crop Protection formulations To formulate, generate scientific / technical data using established systems, procedures, and protocols in an area of work delegated by the manager. Define the experimental programme that include the development of new pesticide formulations, procedures/standards. To interpret data in order to make contributions to decisions in the work programme content, procedures, or problem solution. Engages directly with other functions to co-ordinate delivery of project outputs (e.g. product biology, regulatory, procurement team, engineering team, packaging etc) with the support of a leader. Report on work, including recommendations to project team or sub-project team leader. Participate in regional and global technical / project teams Will represent the formulation development work/status at every developmental stage to global peer review team and adhere to project timelines. ACCOUNTABILITIES To plan, organise and carry out the work programmes at the laboratory, semi-technical, pilot plant or manufacturing scale to design novel pesticide formulation options in order to: Prove the suitability for progression through Stage C and D Evaluation and Development Provide Product Chemistry type and or supporting data, and Provide the formulation design input required to define the process equipment and quality assurance requirements to timescales and specifications agreed with the team or group leader. Ensure the quality of Evaluation and Development formulations by arranging for biological efficacy, toxicology, and hazard assessment studies to be carried out in other Functions. Provide advice and recommendations to allow appropriate selection of formulation manufacturing sites for individual products, together with the product design inputs required to define the process equipment and quality assurance requirements. To interpret and represent to project members external to the function, experimental data and report results and conclusions obtained both orally and in written form to allow cogent and timely Stage C and D project decisions, Regulatory submissions and accurate information archiving and transfer for future commercial manufacturing activities. To ensure that work by the job holder and subordinate staff comply with Syngenta standard operating procedures and statutory regulations (e.g. GLP or similar). To ensure that the jobholder and subordinate staff work safely and healthy with due care for others, so that compliance with Syngenta’s HSE Policy is achieved. To invest in personal and professional development and growth, undertaking, where appropriate, training and development activities and ensuring familiarity with new research and literature. Ensure maintaining complete confidentiality of all Syngenta intellectual property. Interact with the global formulation community in order to better solve common problems and to define improved processes Qualifications KNOWLEDGE EXPERIENCE and CAPABILITIES: Critical knowledge and experience Master’s degree in Pesticide/Agrochemical chemistry must/preferable from reputed universities with strong academic records and good communication skills with > 8 years of industrial experience in field of pesticide formulation development as a formulation development chemist preferred. Thorough knowledge of pesticides, pesticide formulation types and techniques required in formulation development. Sound understanding of agrochemical formulations / Coformulations / Fillers is a must Critical technical, professional, and personal capabilities Ability to efficiently build up laboratory works and experiments Ability to effectively participation in- and contribute to regional / global multi-functional teams Ability to deliver to agreed timelines Excellent operational, organisational, interpersonal and computer skills Sensitive to different cultural environments Self-motivating Critical leadership capabilities Communicative We deliver clear messages to our stakeholders We are keen to listen and learn Team Oriented We model commitment We support team process improvement We collaborate effectively across organisational and functional boundaries Results Oriented We focus on goal achievement We stay focused Customer Focused We seek to understand our customers We build collaborative relationships Trusted We demonstrate support for others Critical success factors and key challenges This role will involve taking a lead role in the development of new formulations by generating potential formulation options through the design of appropriate experimental work programs to thoroughly optimise and test these according to the formulation development process. This will include the analysis of experimental data in order to make inputs to the decisions on the direction of the work programmes within the project. The job holder will need to have experience of different formulation types as well as a full range of broader requirements in formulation development such as product application, manufacturing processes, etc. To deliver highest quality results in optimal time and maintain highest standards of HSE Additional Information Additional Information : People are at the heart of what we do: Once a year Full body check Competitive insurance scheme Employee assistance program – to take care of your and your loved ones mental health Paid Vacation of 30days, 12 Paid Holidays, Maternity and Paternity Leave, compassionate leaves Education assistance – for your career growth People first culture translated into ‘ Most Preferred place to work 2022-23 by Times group’ Note: Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. To learn more visit: www.syngenta.com and www.good-growth-plan Follow us on: Twitter & LinkedIn Twitter LinkedIn

501682 NMSU satellite location, New Mexico, United States Staff Staff Full-time Closing at: Aug 30 2025 - 23:55 MDT Position Title: Dir, Vet Laboratory Employee Classification: Dir,Vet Laboratory College/Division: New Mexico Dept of Agriculture Department: 181300-NMDA VETERINARY DIAGNOSTIC SVC Internal or External Search: External - Open to all applicants Location: NMSU satellite location Offsite Location (if applicable): Albuquerque, New Mexico Target Hourly/Salary Rate: Commensurate with education and experience Appointment Full-time Equivalency: 1.0 Exempt or Non-Exempt : Exempt Summary: New Mexico Department of Agriculture (NMDA) works for the benefit of the state’s citizens and supports the viability of agriculture and affiliated industries. NMDA promotes food protection, a uniform, and fair marketplace, and global marketing and economic development; supports the beneficial use of natural resources; and works cooperatively with public and private sector entities. Opportunities for excellence abound, and NMDA staff dedicate themselves to proactive service in fulfilling the department’s mission. Each division plays an important role in carrying out the goals and objectives. Our rich agricultural history, culture, and traditions are addressed through new and innovative approaches using the latest in science, technology, and economic strategies. In New Mexico, we contribute to the safest and most affordable, and nutritious food supply on the globe. NMDA is a constitutional agency organized under the Board of Regents of New Mexico State University (NMSU). This unique relationship creates efficiencies and opportunities for New Mexico’s food and agriculture sector as well as service and outreach opportunities for NMSU, making NMDA an integral part of the university. NMDA/NMSU is an equal opportunity and affirmative action employer. The Veterinary Diagnostic Services office is located in Albuquerque, New Mexico. Albuquerque is New Mexico's largest city located in the Rio Grande Valley about one hour south from the states capital Santa Fe. Albuquerque's modern downtown core contrasts with Old Town. the surrounding area is filled with plenty of outdoor activities, small towns and plenty of sunshine. This position offers a balance of home and work life. Classification Summary: To direct and manage a multi-program division for the New Mexico Department of Agriculture (veterinary diagnostic laboratory) that has major and direct statewide significance and impact upon agency mission. Agency programs are constitutionally bound by the State of New Mexico and through state statute to promulgate and enforce rules related to specific program areas. Works under minimal supervision and reports directly to the Director/Secretary or Deputy Director/Secretary. Classification Standard Duties: The Division Director administers resource and operational activities to ensure delivery of services or products to citizens and industry. Division Director works closely with the agency director/secretary to establish overall departmental policy, goals, and priorities. The Division Director has extensive latitude for use of independent judgment and initiative. Assigned objectives are broadly defined by statute, grant, and agency mission; routinely interacts with other state, federal, local, tribal counterparts. Requires legislative interaction, initiating, reviewing, and drafting legislation; informing and advising board/committee members and constituents; serves as department representative on assigned issues. Objectives managed have an extensive relationship to the agency mission and require direct accountability, including implementation of strategic direction, budgeting, and assessment. Provide information and interpretation of diagnostic tests and results for submitting clients and veterinarians. Maintain effective liaison with state and federal animal regulatory agencies, in addition to producer groups and veterinary associations within New Mexico and the Southwest. Provide timely information on pertinent animal disease issues to the Director/Secretary and Deputy Director/Secretary. Supervise and evaluate veterinary laboratory personnel. Perform related work as required and other duties as assigned. Required Education, Experience, Certification/License, Equivalency Required Education:Doctorate degree in related field.; Required Experience:Eight (8) years of increasingly progressive management experience in one or more areas that report to this position.; Equivalency:None; Required Certification/License: Knowledge, Skills and Abilities KNOWLEDGE:Knowledge of university and department policies and procedures; local, state, and federal laws, and regulations; agricultural and livestock sector in New Mexico and the United States; regulated industries; specialized knowledge of state government; principles and practices of public administration and fiscal and operational management; livestock diseases and management principles of various food animal producers in New Mexico and the desert Southwest; Good Laboratory Practices; development of standard operating procedures; World Organization of Animal Health (OIE), American Association of Veterinary Laboratory Diagnosticians (AAVLD), and ISO17025 QA/QC recommendations and procedures; overall management needs and requirements of a full-service veterinary diagnostic laboratory and its inherent sub-disciplines (i.e., serology, virology, microbiology, histology, molecular diagnostics, necropsy, pathology, cytology, etc).; SKILLS:Skill in short- and long-range planning and implementation; problem analysis and resolution; evaluating alternatives in decision-making; effective leadership and communication skills; experience and expertise in a veterinary laboratory discipline (i.e., pathology, microbiology, toxicology, molecular diagnostics, etc.); advanced computer usage.; ABILITIES:Ability to select, direct, evaluate, train, and supervise the work of personnel; communicate effectively in written and oral form including public presentations; maintain accurate records; develop and maintain effective relationships; use independent judgment and initiative; take corrective planning action to maintain strategic course of agency mission; oversee various veterinary laboratory sections and participate in analysis and problem solving with section chiefs in their respective sub-disciplines (i.e., serology, virology, microbiology, histology, molecular diagnostics, necropsy, pathology, cytology, etc.) Job Duties and Responsibilities As a full service veterinary diagnostic laboratory, VDS works closely with practicing veterinarians, livestock producers, animal owners, and state and federal agencies. Services provided include necropsy, histopathology, pathology, bacteriology, serology/virology, molecular biology, and immunohistochemistry. As a laboratory, VDS administers all activities through a quality management system incorporating policies and protocols from NMDA and NMSU. In addition to those of the National Laboratory Animal Health Network (NAHLN) and ISO/IEC 17025:2017. Preferred Qualifications Special Requirements of the Position Department Contact: Cheryl Mason-Herrera, 646-7523,cmason@nmda.nmsu.edu Contingent Upon Funding: Contingent upon funding Bargaining Unit Eligibility: This is NOT a bargaining unit position with American Federation of State, County & Municipal Employees (AFSCME). Standard Work Schedule: Standard (M-F, 8-5) If Not a Standard Work Schedule: Working Conditions and Physical Effort Environment: Work is normally performed in a typical interior/office work environment. Physical Effort: No or very limited physical effort required. Lifting Requirements: Requires handling of average-weight objects up to 10 pounds or some standing or walking. Risk: No or very limited exposure to physical risk.

You will be responsible for leading genotoxicity studies such as the Bacterial Reverse Mutation test (AMES), Bone Marrow Micronucleus Test, Chromosome Aberration Test, and In vitro Micronucleus Test as a Study Director in the Toxicology (Genotoxicology) field. Additionally, you will also act as Study Personnel for general toxicology studies. Your main duties will include preparing study plans, amending study plans, creating study reports, developing and reviewing Standard Operating Procedures (SOPs), and maintaining the in vitro laboratory. You will also assist in departmental activities as needed and partake in the validation of new assays to enhance our capabilities. You will be involved in conducting various assays such as the hERG assay, hepatotoxicity assays, and miniature Ames tests. Furthermore, you will handle the cryopreservation, maintenance, and handling of strains/cell lines, as well as slide preparation, staining, coding, decoding, analysis, and data compilation for studies like MNT and Chromosome aberration. Your responsibilities will also include compiling, verifying, and statistically analyzing study data, managing the handling, storage, and disposal of positive control items related to genotoxicity studies, and operating and maintaining laboratory equipment used in non-clinical safety studies. In addition to technical skills, soft skills such as excellent planning, interpersonal, problem-solving, and communication skills are essential for this role. Proficiency in MS Office is considered desirable for the position.,

As a candidate for the position, you should possess a M. Pharm (Pharmacology/ Pharmaceutical Analysis) or M.Sc. (Biochemistry/ Pharmaceutical Chemistry) degree with 11-14 years of experience or a Ph.D. with 2-5 years of experience in the fields of large molecule/ADC PK and bioanalysis. Your expertise should include Antibody Drug Conjugate characterization and bioanalysis, mass spectrometry-HRMS, Q-TOF, and Triple quad. Your role will involve being an expert in designing and executing DMPK studies to support antibody-drug conjugate (ADC) and monoclonal antibody (mAb) programs, ranging from discovery to IND-enabling stages. You should have extensive experience in quantifying biologics such as antibodies, therapeutic proteins, ADCs, and peptides using LC-MS/MS, MSD, and ELISA platforms. Proficiency in advanced bioinformatics tools like BioPharma Finder, MaxQuant, Spectronaut, and other relevant analytical software is essential. Your responsibilities will also include applying innovative techniques for identifying and selecting ADC and mAb lead candidates based on their functions, with a strong emphasis on DMPK profiling to ensure the safe and effective development of therapeutics. You should be adept at interpreting complex DMPK data and providing actionable insights to cross-functional project teams. Active representation of DMPK functions in internal and external meetings to promote collaboration and strategic alignment is crucial. Collaboration with cross-functional departments to address ADC-related challenges and provide integrated solutions from target validation to IND submission will be part of your role. You will be accountable for authoring and reviewing SOPs, study protocols, reports, and regulatory documentation to support both GLP and non-GLP studies. A strong foundational knowledge of DMPK principles including PK/PD, toxicology, and translational sciences is required. Demonstrated capabilities in communication, innovation, and team leadership will be essential for success in this position.,

As a Toxicologist / Preclinical Scientist at our organization, you will play a crucial role in conducting toxicological risk assessments and overseeing preclinical experimental research. Your responsibilities will include deriving health-based exposure limits, conducting toxicological risk assessments for various substances, performing genotoxicity hazard assessments, evaluating extractable and leachable impurities, and determining harmful doses for children. In addition, you will be involved in developing preclinical strategies, planning, overseeing, and interpreting in vitro and in vivo preclinical toxicology studies, pharmacokinetics/pharmacodynamics studies, biocompatibility studies for medical devices, and immunogenicity studies for peptides and biosimilar products. You will also be responsible for summarizing toxicological data and preparing regulatory submissions such as Investigational Brochures, Investigational New Drug applications, and electronic Common Technical Document for regulatory authorities. To qualify for this role, you should have an advanced degree in Toxicology, Pharmacology, Zoology, Veterinary Medicine, or a related field, along with a minimum of 3-5 years of experience in toxicological risk assessment and experimental toxicology in the pharmaceutical, CRO, or biotechnology industry. You must possess a strong understanding of regulatory guidelines from organizations such as ICH, USFDA, EMA, CFDA, and DCGI, and have experience with regulatory submissions. Furthermore, you should demonstrate the ability to manage multiple projects simultaneously, work effectively in a dynamic team environment, communicate excellently, collaborate cross-functionally, and interact with external partners such as CROs. Being detail-oriented with proactive planning abilities, strong analytical skills, effective timeline management, adept problem-solving capabilities, and excellent collaboration and teamwork skills are essential for this role. Proficiency in using computer software including Microsoft Office suite, SharePoint, QSAR tools, data mining software, citation tools, and other relevant applications is required. This full-time position is based in Vikhroli, Mumbai, with general shift hours and rare/occasional travel for outdoor duties/monitoring.,

The role of General Manager, Veterinary Sciences at Syngene International Ltd. in Bangalore is a highly strategic position responsible for leading the BBRCs in vivo research operations. As the Head of Veterinary Sciences, you will oversee a 50,000 sq. ft. AAALAC-accredited facility supporting various therapeutic and functional areas. Reporting to BMS Veterinary Sciences leadership and the Head of Site Operations, you will play a crucial role in the BBRC Operations Leadership Team. Your main responsibilities will include ensuring high-quality support for in vivo pharmacology, DMPK, toxicology, and translational research within the Veterinary Sciences BBRC function. You will collaborate with global stakeholders to align strategies across R&D sites and drive long-term strategies to develop capabilities and capacity in support of BMS drug discovery portfolio. As a leader, you will be responsible for coaching and developing a multidisciplinary team to meet departmental objectives while fostering a culture of excellence, collaboration, accountability, and continuous learning. Oversight of local aspects of veterinary care, animal welfare, and vivarium operations to ensure compliance with international regulations and BMS standards will also be part of your role. Your qualifications should include a PhD in Veterinary Science (a plus), board certification in Laboratory Animal Medicine, eligibility for veterinary licensure in India, and at least 15 years of experience in laboratory animal medicine with leadership roles in pharmaceutical or research settings. Additionally, you should have expertise across multiple species used in pharmaceutical research, strategic acumen in managing vivarium and veterinary functions, strong interpersonal and communication skills, and the ability to manage multiple projects with resilience and emotional intelligence. Preferred attributes for this role include operational leadership of multi-site or global veterinary functions, scientific innovation in developing in vivo disease models, and a passion for ethical research, leadership, and high-performing team development. Syngene International Ltd. is an equal opportunity employer committed to fostering a diverse and inclusive workplace.,

The Senior Business Development Executive position at Ribosome Research Center in Kim, Surat requires a candidate with an MBA in Marketing and 5 to 10 years of experience working as a Business Development Executive in a Contract Research Organisation. The ideal candidate should have experience in GLP, Pre Clinical or a well-known CRO Company. As a Senior BD Executive, you will be responsible for developing strategic market positioning and creating market space. You will be expected to generate new leads for contract research services and create effective market campaigns in Preclinical R & D, Pharma R & D, drug testing, toxicology, and analytical testing. Additionally, you will be managing key global strategies and collaborating with the research team to develop services of the Contract Research Organisation aligning to the needs of OECD GLP compliances. Your role will also involve managing existing businesses and creating long-term business opportunities. The benefits of this position include food provided, leave encashment, paid sick time, and paid time off. Key skills required for this role include business development, research, CRO management, toxicology, lead generation, contract research services, pharma R&D, business opportunities, market positioning, OECD GLP compliance, preclinical, drug testing, campaigns, analytical testing, and strategic planning.,

Role: Product Manager Department: DPEx Role Band: S - equivalent to Indigo Location: Miyapur, Hyderabad No. of Positions: - 01 Context APSL has embarked on an organization wide initiative of Business Transformation & Process Excellence leveraging Digital, Analytics & Automation. The DPEx team plays a key role in understanding business processes, suggesting solutions and planning & executing these solutions to create direct impact on business KPIs. The Product Manager is expected to lead many such initiatives within the organization. The product manager should understand the business requirements, map processes, translate business & process requirements into business requirement specifications and drive business excellence initiatives. He/she should work collaboratively with cross functional teams (CFTs), own/co-own & drive internal projects & products. What makes this assignment interesting ? Broader understanding of APSL business context and scenarios Opportunity to own & create new business platforms and drive impact on P&L Insight into the Business workings & process related to RnD labs (PRD, ARD, FRD, Process Engineering, Drug Discovery labs (MedChem, DMPK, Animal Toxicology, Cellular & Molecular Biology, etc.)) Value chain analysis and understanding of latest trends in business applications. Key Responsibilities Lead Digital initiatives end-to-end from ideation to execution and adoption Responsibility to own the business metrics and its delivery through direct and vendor-led work around internal products Develop clear roadmap & strategy to improve business KPIs and user experience Participate in business user requirements and understand the key operational & data challenges of the organization. Prepare business processes documents, URS and recommendations related to proposed solution. Adoption tracking and reporting to senior management. Develops functional specifications and system design specifications for client engagements. Oversee development of solution prototype. Ensures issues are identified, tracked, reported on and resolved in a pro-active manner. Communicates needed changes to development team. Technical Requirements Must have good technology inclination, exposure to business applications like ELN, Empower, etc. Must have hands-on experience in Designing, solutioning & executing Digitization projects/products, process improvement projects Should have played a BA+ Product Manager role for at least 3-5 years Good understanding of business processes in at least one of the functions like Pharma R&D , Lab Automation, Drug discovery & development. Exhibits confidence and an extensive knowledge of emerging industry practices when solving business problems. Knowledge in Product management background and familiar with PMI project methodologies and SDLC. Must have hands-on experience in process mapping, creating URS & specification documents & project management. Education & Experience BTech + MBA would be preferred. Prefer minimum 3-5 years of experience in Product Management of business applications around Pharma R&D Services, CDMO, Discovery or in a consulting firm.

Serve as the single point of scientific, administrative and regulatory control for the study Participate and oversee all study activities (animal dosing, clinical signs observation, other relevant procedures, data collection, data analysis etc.,) in accordance with applicable regulations, OECD Principles of GLP and relevant SOPs Operation, maintenance and usage of relevant equipment/instruments used (ex. centrifuge, laminar air flow, anesthetic machine, weighing balances, refrigerator, deep freezers, syringe pumps etc). Preparation and revision of SOPs applicable to in vivo and in vitro experiments/procedures Communicate critical information to key study personnel, the sponsor, and to responsible scientists as applicable Authorize amendments and deviations to the study plan as applicable Respond to QA findings and resolve them in a timely manner Approval of study plan, amendments and study reports Responsible for the timely archival of the study as per the current practices All responsibilities as Study Director in accordance with the applicable SOPs

Job Description: Specialist position in Toxicology (Genotoxicology) Function as Study Director for genotoxicity studies such as Bacterial Reverse Mutation test (AMES), Bone Marrow Micronucleus Test, Chromosome Aberration Test and In vitro Micronucleus Test. Function as a Study Personnel for general toxicology studies. Preparation of study plan, study plan amendment, study report, SOPs and their review Maintenance of in vitro laboratory and assist in departmental activities as necessary. Perform validation of new assays as a part of capability building. Conduct of hERG assay, hepatotoxicity assays, miniature Ames tests etc. Cryopreservation, maintenance and handling of strains/cell lines. Slide preparation, staining, coding, decoding, analysis and data compilation for MNT and Chromosome aberration studies. Compilation, verification and statistical analysis of study data. Handling, storage and disposal of positive control items pertaining to genotoxicity studies. Operation and maintenance of lab equipment used in non-clinical safety studies. Soft skills: Excellent in planning, interpersonal, problem solving and communication skills Proficiency in MS office is desirable

Job description for a Scientist position in General Toxicology as below: Function as Study Director for general toxicology studies (acute, repeated dose toxicity studies and PK studies). Function as a Study Personnel for general toxicology studies conducted by other Study Directors. Preparation of study plan, study plan amendment and deviations, study report, SOPs and their review Maintenance of in vivo laboratory and assist in departmental activities as necessary. Perform validation of new studies as a part of capability building. Compilation, verification and statistical analysis of study data. Procurement, handling, storage and disposal of chemicals/ items pertaining to general toxicity studies. Operation and maintenance of lab equipment used in non-clinical safety studies. Liaise with QA for GLP studies and facility compliance.

Role & responsibilities: 1. Act as Study Director for various Pre-Clinical studies as per guidelines 2. Conduct, schedule & report toxicological studies for various products in pre-clinical studies 3. Conduct Pharmacological evaluation of various pharmaceutical products 4. Preparation of SOP & documentation as per guidelines 5. Ensuring facility readiness as per regulatory guidelines & audits Preferred candidate profile: Local candidates

Job Description Job Title : HOD - Regulatory Affair Education : B.Sc. /M.Sc. (Agrochemicals, Chemistry) Location: Ahmedabad Roles And Responsibility:- Responsible for data generation of toxicology/ecotoxicology, microbiology studies according to OECD/CIPAC/SANCO/CDSCO international guidelines for the regulatory submissions of the agrochemicals in LATAM, Brazil, USA and other countries. Responsible for managing the regulatory process of agrochemical products and ensuring the compliance with international laws and regulations. Collaborate with R&D teams to develop new pesticide products or formulations. Monitor product performance, develop and execute sales strategies to achieve revenue. Establish relationship with customers across the globe and conduct business meetings with clients. Successfully manage the preparation and submission of regulatory dossiers, achieving timely approval and market access. Liase with global GLP laboratories to generate and interpret data for product registration. Also work closely with universities and research institutions to generate scientific data supporting product applications. Oversee the regulatory registration process for agrochemical products in multiple countries. Maintain up-to-date Toxicology, Chemistry, Packaging etc. plans for all projects/programs/products, including listings of studies, timelines, status and costs, update and refine as necessary to meet the committed timelines. Strengthening company relationships with government and regulatory bodies in order to ensure supportive political and regulatory environment for business growth. Developing regulatory strategies to obtain regulatory approvals with USA, EU, LATAM, AUSTRALIA and other International Agencies. Also working for Indonesia, Malaysia, Mexico, Philippines, Nepal, Bangladesh, Taiwan, Vietnam and African countries etc. Successfully manage the preparation and submission of regulatory dossiers, achieving timely approval and market access. Managed budget for regulatory activities ensuring cost effective use of resources.

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. This position focuses on collecting data on chemical substances from published regulatory or industry association sources. Examples include international inventory lists, occupational exposure limits, GHS classification lists, environmental emission restrictions (air, water, waste), transport of dangerous goods, and physical properties among other types of data. Roles And Responsibilities Proactively monitor legislation maintained by Sphera by reviewing regulatory standards and interpretations, registers, gazettes, newsletters, etc. as related to Regulatory Data Content. Identify applicable new and updated/revised legislation and obtain official source documents. Analyze regulations for inclusion in Regulatory Content database. Develop and maintain technical documentation (in pre-defined templates) that clearly describes the analysis and interpretation of the Regulatory Data Lists. Perform assigned data maintenance projects for a repository of over 230,000 regulated chemical substances. Be fully accountable for the individual update assignments in terms of quality and schedule. Develop and maintain effective relationships with regulatory agency contacts and consultants specializing in specific regulations. Liaise with Content Development, Rules, QA, product management and other teams to identify and implement continuous improvement initiatives for content quality and work process efficiency enhancements. Attend weekly meetings with the Regulatory Data Analysts/Data team. Required Education University degree in Chemistry, Toxicology, Ecology or related fields. University or Advanced degree or professional certification in a related field is considered an asset. Preferred Experience 0-2 years of experience working with EHS regulations or practical experience working with chemicals. Experience working with relational databases using programs such as MS Access or SQL. Experience with data manipulation in MS Excel. Experience with other MS office programs. Good knowledge of chemical nomenclature and chemical structures. Fluent in English (both spoken and written) and strong reading/writing skills. Preferable knowledge of any other languages (i.e. French, German, Spanish or a language from Eastern Asia). Other Skills Knowledge of global chemical regulations and GHS; experience authoring Safety Data Sheets will be an advantage. Ability to assign chemical substances to applicable chemical groups based on properties such as solubility, metal content, petroleum streams, etc. will be an advantage. High level of attention to detail. High level of initiative. Flexible, adaptable to change. Excellent organizational, time-management and prioritization skills. Excellent interpersonal and communication skills. Physical Requirements: Ability to physically perform general office requirements. Must be able to perform essential responsibilities with or without reasonable accommodations. Sphera is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. This job description is intended to convey information essential to understanding the scope of the job and the general nature and level of work performed by job holders within this job. This job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities or working conditions associated with the position.

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Job Description Job Summary Job Title – Research Scientist - I Location – Whitefield, Bangalore Shift – General Your Role At Vantive The successful candidate for this role will be part of the Analytical Chemistry and Stability (ACS) team and will bring hands-on and technical leadership experience in Elemental analysis for medical devices and drug products. This Research Scientist role will entail utilization of expertise in analytical chemistry, Atomic Absorption (AA), Inductive Coupled Plasma techniques (ICP-OES, ICP-MS) and other appropriate techniques to perform gap assessments for medical device and drugs requirements and support change control activities across the Renal and Acute Care businesses within Vantive. The successful candidate is expected to also have a strategic mindset and will work closely with regulatory, quality, preclinical and product design owning leaders to enable investigations of trace level Elemental Analysis in drugs & devices to support on-market or new product programs. This role will also include planning and performing laboratory work in AA, ICP-MS and ICP-OES, including independent execution of laboratory studies at in-house or external labs for Method Development and Validations. The candidate will likely act as study director for multiple studies at any given time and is expected to be able to do wet chemistry, AA, ICP-MS and ICP-OES hands-on as required from time to time for efficient and effective execution of the program. The individual will author required reports (internal documentation and regulatory submissions) following pertinent internal and external guidelines that ensures safety and compliance of drugs or devices that Vantive makes. The candidate is expected to stay abreast of emerging sciences and technologies that influence chemical characterization for medical devices and drugs through active participation in relevant external forums / societies. Essential Duties And Responsibilities. Develop strategies to effectively apply a risk-based scientific approach within a regulatory framework to support trace level Elemental analysis projects and change control activities. Develop and Validate Methods for Elements and Elemental Impurities using the ICP-OES, ICP-MS and other relevant techniques. Define strategy for conversion of legacy AA methods to ICP and prove the equivalency between two techniques by following appropriate statistical methodologies. Collaborate with a multidisciplinary team of subject matter experts (e.g. ACS, E&L, Materials, Biocompatibility, and Toxicology) to develop trace level Elemental analysis strategies that align to regulatory requirements for medical devices and drug products. Participate in ACS change control impact assessments when applicable to trace Elemental impurities analysis and work with cross functional team members (design owners, E&L SMEs, materials, preclinical, etc.) to determine a comprehensive testing strategy through writing impact assessments, gap assessments, technical rationales and documents related to such change controls. Maintain and apply current knowledge of relevant Quality System Regulations and other regulatory requirements related to chemical characterization of product development, design and safety. Interact across functions (Design Owning Organization, Project Management Organization, Regulatory Affairs, Preclinical, etc.) to understand products and therapies, as well as business, technical, and regulatory requirements to meet project needs. Should have knowledge, experience, and responsibilities on the matter that are essential for ensuring Manufacturing Plants can escalate and share any concerns regarding compliance to quality system for “Management and Control of Elemental Impurities” and “Elemental Impurity Risk Assessments”. Qualifications. Demonstrated experience in applying Elemental Impurity analysis methods and tools as part of R&D Knowledge of regulatory expectations related to Elemental analysis for drugs and devices. Performing change control in a GMP environment. Experience in working in global cross-functional teams for trace Elemental Impurities analysis projects independent problem solver who can use a methodical approach to develop solutions and make recommendations. Education And/or Experience. Bachelor’s degree in scientific discipline (Analytical or Organic chemistry preferred) with a minimum 14 years of experience, or MS with a minimum 7 years of experience or PhD with a minimum 3 years of relevant experience. Reasonable Accommodation Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

Job Description: Toxicologist / Preclinical Scientist We are seeking a skilled Toxicologist / Preclinical Scientist to join our team. The ideal candidate will be accountable for conducting toxicological risk assessments and overseeing preclinical experimental research. 1. Key Responsibilities: Toxicological Risk Assessments • Derive Health-based Exposure Limits & support occupational hazard assessment (PDE/OEL) for pharmaceutical molecules in adherence to regulatory standards. • Conduct Toxicological Risk Assessments (TRA) for pharmaceuticals, excipients, intermediates, chemicals, cleaning agents, residual solvents, elemental impurities, and degradation products. • Perform Genotoxicity Hazard Assessments for impurities using published or experimental in-vitro/in-vivo data and in-silico (Q)SAR tools according to ICH M7 guidelines. • Evaluate extractable and leachable impurities using literature review and in-silico tools. • Determine Harmful Doses for children to guide selection of blister packaging. 2. Key Responsibilities: Experimental Toxicology & Preclinical Research • Develop preclinical strategies supporting differentiated product development. • Plan, outsource, oversee, and interpret in vitro and in vivo preclinical toxicology and pharmacokinetics/pharmacodynamics (PK/PD) studies for complex/differentiated products and impurity qualifications. • Plan, outsource, oversee, and interpret in vivo/ in vitro biocompatibility studies for medical devices. • Plan, outsource, oversee, and interpret in vitro immunogenicity studies for peptides and biosimilar products. • Summarize toxicological data and prepare Investigational Brochures (IBs), Investigational New Drug (IND) applications, and electronic Common Technical Document (e-CTD) for regulatory authority submissions. Qualifications and Skills • Advanced degree in Toxicology, Pharmacology, Zoology, Veterinary Medicine or related field. • Minimum 3-5 years of experience in toxicological risk assessment & experimental toxicology within the pharmaceutical, CRO or biotechnology industry. • Strong understanding of regulatory guidelines (e.g., ICH, USFDA, EMA, CFDA, DCGI) and experience with regulatory submissions. • Proven ability to manage multiple projects simultaneously and work effectively in a dynamic team environment. • Excellent communication skills with the ability to collaborate cross-functionally and interact with external partners such as CROs. • Detail-oriented with proactive planning abilities, coupled with strong analytical skills, effective timeline management, adept problem-solving capabilities, and excellent collaboration and teamwork skills. • Skilled in using computer software including Microsoft Office suite (Word, Excel, PowerPoint), SharePoint, QSAR tools, data mining software, citation tools, and other relevant applications. Operational details: • Location: Vikhroli, Mumbai. • Mode: Full time, work from office • Shifts: General shift (8 hours) • Travelling: Rare/Occasional for outdoor duties/ monitoring

As a Principal Scientist within the Preclinical Safety (PCS) Pathology Team at Novartis, you will play a crucial role in advancing translational safety omics data analysis to support innovative drug discovery and development efforts. Your responsibilities will involve collaborating closely with pathologists, bench scientists, and subject matter experts across different Novartis sites such as the USA and Switzerland. Your expertise in omics-based data science and your dedication to enhancing multimodal data analysis in translational drug safety will be key to success in this role. Your day-to-day tasks will include using machine learning and statistical methods to analyze spatial transcriptomics and spatial proteomics data from raw reads, comparing and contrasting different omics data sets, conducting multimodal analysis with other data modalities, and supporting various projects with data science expertise in fields like gene and cell therapy, target discovery, genetics, drug safety, and compound screening. Additionally, you will be expected to innovate by leveraging Data Science and Artificial Intelligence to solve problems effectively, communicate regularly with stakeholders, evaluate new technologies and scientific software, and independently identify and apply research articles to business problems. To qualify for this position, you should hold a Master's or Ph.D. in Data Science, Computational Biology, Bioinformatics, or a related discipline. You must be proficient in programming languages and data science workflows such as Python, R, Git, UNIX command line, and high-performance computing clusters. A minimum of 5 years of experience in analyzing large biological datasets in a drug discovery/development or academic setting is required, along with proven expertise in exploratory data analysis, statistical inference, and machine learning algorithms. Your collaborative mindset, exceptional communication skills, and ability to work in an agile environment will be essential for success in this role. Novartis is a company dedicated to improving and extending people's lives, with a strong belief in the power of medical science and digital innovation. The organization values diversity, equity, and inclusion, fostering an environment that encourages new ways of working and collaboration. By joining Novartis, you will have the opportunity to work in an unbossed culture that promotes integrity, curiosity, and flexibility, allowing you to tackle challenging medical problems with courage and ambition. Novartis is committed to creating an inclusive work environment that reflects the diversity of the patients and communities it serves. If you are interested in exploring career opportunities at Novartis, you can join the Novartis Network to stay connected and receive updates on future roles that align with your goals. Novartis offers a range of benefits and rewards to support your personal and professional growth. To learn more about the opportunities available and the company's commitment to helping you thrive, you can refer to the Novartis handbook on benefits and rewards.,

Mission The Product Steward Specialist is responsible for achieving the company s Product Stewardship objectives for Calderys. This position requires interaction with customers, suppliers, global government agencies, industry associations and employees at all levels within the organisation. This role has overall responsibility for the product stewardship programs, ensuring that business objectives and compliance requirements are met. He/she supports the organisation to contribute to business growth and sustainability regarding all aspects of product stewardship including product compliance, material and product safety, Product Carbon Footprint. The successful candidate is part of the Global Product Stewardship team and will play a critical role in the delivery of Hazard Communication documentation to various internal/external stakeholders and support the Calderys APAC licence to operate. Responsibilities Authoring Safety Data Sheets (SDS s) at regional & global level through the use of an professional software. Regional & Global regulatory monitoring of Safety Data Sheets regulations development, impact assessment on the SDS s portfolio and roll-out of a compliance plan to ensure Calderys APAC conformity Accountable for the compliant product labelling development & communication to APAC manufacturing sites Authoring of safe use, handling and disposal instructions in collaboration with EHS colleagues for further deployment at the APAC manufacturing sites Track and timely respond external customers product stewardship enquiries Accountable for ensuring product compliance & safety testing plan in close collaboration with Innovation& technology and APAC manufacturing sites Ensure product compositional data are up to date and reliable in close collaboration with Product Data, Purchasing and QC Managers Is the PS Single Point of Contact (SPOC) for specific product lines and provides support to internal stakeholders on Product Stewardship matters. Support Innovation and sustainability effort of the APAC from a Product Stewardship perspective Ensure adequate management, storage and retention of Product Stewardship data and knowledge as well as keeping product compliance files up to date Help to maintain PS awareness within the APAC region through communication, training and coaching on Product Stewardship expertise matters Help APAC business area to improve and/or adopt process and new IT tools Identify and foster continuous improvements to increase Product Stewardship team effectiveness, and eliminate non-value-added work for the team and the business is involved into specific PS expertise activities such as Global Chemical and Product Safety regulations monitoring, Chemicals of concerns regulatory monitoring Assist the other Product Stewardship Team Members in various compliance projects and initiatives both at regional or global level Requirements Master s degree in a relevant scientific discipline (chemistry, environmental science, toxicology, material science) Years in a regulatory or product stewardship role, preferably at global industry level focusing on Hazard communication compliance management is a plus Knowledge of SDS authoring software usage is highly recommended Knowledge of SDS regulations and associated requirements at global level coupled with a proven efficiency of hazardous classification determination according to national and GHS regulations. Strong customer service focus & business acumen Advocate for data integrity and management Good organisational, leadership and discipline skills Good written and communication skills. Proficiency in English Strong interpersonal skills and ability to build positive networks with internal/external stakeholders Ability to work independently as part of a growing dynamic team Experience in project management would be a plus

Job Description Job Summary Job Title Research Scientist - I Location Whitefield, Bangalore Shift General Your Role at Vantive: The successful candidate for this role will be part of the Analytical Chemistry and Stability (ACS) team and will bring hands-on and technical leadership experience in Elemental analysis for medical devices and drug products. This Research Scientist role will entail utilization of expertise in analytical chemistry, Atomic Absorption (AA), Inductive Coupled Plasma techniques (ICP-OES, ICP-MS) and other appropriate techniques to perform gap assessments for medical device and drugs requirements and support change control activities across the Renal and Acute Care businesses within Vantive. The successful candidate is expected to also have a strategic mindset and will work closely with regulatory, quality, preclinical and product design owning leaders to enable investigations of trace level Elemental Analysis in drugs & devices to support on-market or new product programs. This role will also include planning and performing laboratory work in AA, ICP-MS and ICP-OES, including independent execution of laboratory studies at in-house or external labs for Method Development and Validations. The candidate will likely act as study director for multiple studies at any given time and is expected to be able to do wet chemistry, AA, ICP-MS and ICP-OES hands-on as required from time to time for efficient and effective execution of the program. The individual will author required reports (internal documentation and regulatory submissions) following pertinent internal and external guidelines that ensures safety and compliance of drugs or devices that Vantive makes. The candidate is expected to stay abreast of emerging sciences and technologies that influence chemical characterization for medical devices and drugs through active participation in relevant external forums / societies. Essential Duties and Responsibilities. Develop strategies to effectively apply a risk-based scientific approach within a regulatory framework to support trace level Elemental analysis projects and change control activities. Develop and Validate Methods for Elements and Elemental Impurities using the ICP-OES, ICP-MS and other relevant techniques. Define strategy for conversion of legacy AA methods to ICP and prove the equivalency between two techniques by following appropriate statistical methodologies. Collaborate with a multidisciplinary team of subject matter experts (e.g. ACS, E&L, Materials, Biocompatibility, and Toxicology) to develop trace level Elemental analysis strategies that align to regulatory requirements for medical devices and drug products. Participate in ACS change control impact assessments when applicable to trace Elemental impurities analysis and work with cross functional team members (design owners, E&L SMEs, materials, preclinical, etc.) to determine a comprehensive testing strategy through writing impact assessments, gap assessments, technical rationales and documents related to such change controls. Maintain and apply current knowledge of relevant Quality System Regulations and other regulatory requirements related to chemical characterization of product development, design and safety. Interact across functions (Design Owning Organization, Project Management Organization, Regulatory Affairs, Preclinical, etc.) to understand products and therapies, as well as business, technical, and regulatory requirements to meet project needs. Should have knowledge, experience, and responsibilities on the matter that are essential for ensuring Manufacturing Plants can escalate and share any concerns regarding compliance to quality system for Management and Control of Elemental Impurities and Elemental Impurity Risk Assessments . Qualifications. -Demonstrated experience in applying Elemental Impurity analysis methods and tools as part of R&D -Knowledge of regulatory expectations related to Elemental analysis for drugs and devices. -Performing change control in a GMP environment. -Experience in working in global cross-functional teams for trace Elemental Impurities analysis projects - independent problem solver who can use a methodical approach to develop solutions and make recommendations. Education and/or Experience. Bachelor s degree in scientific discipline (Analytical or Organic chemistry preferred) with a minimum 14 years of experience, or MS with a minimum 7 years of experience or PhD with a minimum 3 years of relevant experience.

Mission The Product Steward Specialist is responsible for achieving the company s Product Stewardship objectives for Calderys. This position requires interaction with customers, suppliers, global government agencies, industry associations and employees at all levels within the organisation. This role has overall responsibility for the product stewardship programs, ensuring that business objectives and compliance requirements are met. He/she supports the organisation to contribute to business growth and sustainability regarding all aspects of product stewardship including product compliance, material and product safety, Product Carbon Footprint. The successful candidate is part of the Global Product Stewardship team and will play a critical role in the delivery of Hazard Communication documentation to various internal/external stakeholders and support the Calderys APAC licence to operate. Responsibilities Authoring Safety Data Sheets (SDS s) at regional & global level through the use of an professional software. Regional & Global regulatory monitoring of Safety Data Sheets regulations development, impact assessment on the SDS s portfolio and roll-out of a compliance plan to ensure Calderys APAC conformity Accountable for the compliant product labelling development & communication to APAC manufacturing sites Authoring of safe use, handling and disposal instructions in collaboration with EHS colleagues for further deployment at the APAC manufacturing sites Track and timely respond external customers product stewardship enquiries Accountable for ensuring product compliance & safety testing plan in close collaboration with Innovation& technology and APAC manufacturing sites Ensure product compositional data are up to date and reliable in close collaboration with Product Data, Purchasing and QC Managers Is the PS Single Point of Contact (SPOC) for specific product lines and provides support to internal stakeholders on Product Stewardship matters. Support Innovation and sustainability effort of the APAC from a Product Stewardship perspective Ensure adequate management, storage and retention of Product Stewardship data and knowledge as well as keeping product compliance files up to date Help to maintain PS awareness within the APAC region through communication, training and coaching on Product Stewardship expertise matters Help APAC business area to improve and/or adopt process and new IT tools Identify and foster continuous improvements to increase Product Stewardship team effectiveness, and eliminate non-value-added work for the team and the business is involved into specific PS expertise activities such as Global Chemical and Product Safety regulations monitoring, Chemicals of concerns regulatory monitoring Assist the other Product Stewardship Team Members in various compliance projects and initiatives both at regional or global level Requirements Master s degree in a relevant scientific discipline (chemistry, environmental science, toxicology, material science) Years in a regulatory or product stewardship role, preferably at global industry level focusing on Hazard communication compliance management is a plus Knowledge of SDS authoring software usage is highly recommended Knowledge of SDS regulations and associated requirements at global level coupled with a proven efficiency of hazardous classification determination according to national and GHS regulations. Strong customer service focus & business acumen Advocate for data integrity and management Good organisational, leadership and discipline skills Good written and communication skills. Proficiency in English Strong interpersonal skills and ability to build positive networks with internal/external stakeholders Ability to work independently as part of a growing dynamic team Experience in project management would be a plus

Responsibilities : - Conduct comprehensive toxicology risk assessments across diverse scenarios, ensuring robust safety evaluations. Conduct & review of toxicology risk assessments for excipients, impurities, solvents, extractables and leachables, ensuring adherence to regulatory standards. Execute Environmental Risk Assessments (ERA) in compliance with the latest EMA guidelines. Prepare, maintain, and update toxicology summaries for globally marketed products in alignment with company policies. Develop and compile PDE and OEL monographs to support safety evaluations. Prepare clinical and non-clinical dossier modules (Modules 2.4, 2.5, 2.6, 2.7, 4, and 5) for regulatory submissions. Manage preclinical studies and associated documentation to ensure compliance and accuracy. Perform QSAR genotoxicity assessments in accordance with ICH M7 guidelines. Utilize advanced in-silico predictions (DEREK, SARAH, NEXUS, TOXTREE, OECD Toolbox) for data analysis and risk assessment. Provide expert guidance in addressing client and regulatory inquiries effectively. Background Required - Qualified Toxicologist Signing non-clinical/ toxicological reports/ modules/ expert reports Drafting of Environmental risk assessment reports Due diligence of pre-clinical data and drafting strategy for non-clinical studies for complex generics, NCEs, Biologics etc Drafting and review of non-clinical CTD modules Drafting of PDE reports Toxicological risk assessment of impurities/ leachables/ extractables Required education: Qualified and experienced Toxicologist Required experience : At least 2 years of experience in above mentioned activities.

Dear All, Greetings from Vivo Bio Tech Limited! Job Description: Business Development (BD) role** in a CRO setting Experience: 3+ Job Title:** Business Development/Executive/ Manager/Sr. Manager_ Preclinical Services Location:** Hyderabad Reports To:** Head Business Development / Executive Director Job Overview: We are seeking a proactive and results-driven **Business Development Manager** to independently drive lead generation and conversion across domestic and international markets. The ideal candidate should have strong networking skills within the **CRO industry**, and proven experience in securing business from **Pharma, Agrochemicals, Industrial Chemicals, Vaccines, Generics, and Medical Devices** clients. This role requires working knowledge of **GLP compliance**, **regulatory affairs**, **toxicology studies**, and familiarity with submission processes to global regulatory bodies. Key Responsibilities:** * Independently generate, qualify, and convert leads for preclinical research services. * Submit tailored technical and commercial quotations to potential clients. * Network extensively across Pharma, Agrochemical, Vaccine, Generic Drug, Medical Device, and Chemical industries. * Understand client requirements and align them with organizational capabilities in **GLP and non-GLP studies**. * Develop and maintain strong client relationships to drive repeat and long-term business. * Coordinate with internal scientific and operational teams to design study proposals and timelines. * Provide market intelligence and competitor analysis to support strategic planning. * Track, monitor, and support **regulatory submissions** to international authorities such as USFDA, EMA, WHO, PMDA, ANVISA, etc. * Stay updated with global guidelines relevant to **Mammalian Toxicology**, **Ecotoxicology**, and **Regulatory Submissions**. * Promote services across **small and large animal studies**, including rodent, canine, minipig, and non-human primate models. * Collaborate on proposals for government and international grants or tenders (if applicable). Key Requirements:** * Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related fields. * Minimum 2–15 years of BD experience in a CRO or related preclinical research setting. * Strong understanding of **GLP requirements** and study types. * Working knowledge of **toxicology, pharmacology, ecotoxicology**, and **regulatory pathways**. * Familiarity with **GTC (General Toxicity Category)** studies and their scope. * Excellent communication, negotiation, and relationship-building skills. * Self-motivated and target-oriented with strong business acumen. * Willingness to travel domestically and internationally as required. --- Preferred Experience: * Exposure to **OECD, ICH, USFDA, EPA, REACH, and other regulatory guidelines**. * Experience in handling **multi-national clients** and long-term contracts. Vivo Bio Tech Ltd Survey # 349/A, Pregnapur Village, Gajwel Mandal. Siddipet District, PIN 502311,Telangana, India. Regards, Chandra Kanth | HRD chandrakanth.k@virinchi.com

Employment Offer Drug Discovery and Development Division at Patanjali Research Foundation, Haridwar, INDIA Patanjali Research Foundation is a fully integrated, innovative research institute to conducts modern experimentation on Ayurvedic medicines for the treatment of various diseases. The Institute has a diversified research portfolio and a substantial clinical testing pipeline. With its R&D centre and headquarters in Haridwar, India, Patanjali also has a mega manufacturing facility, an Ayurvedic hospital and medical college, a University, and a herbarium along with an herbal garden. Research laboratories at Patanjali are accredited with NABL, DSIR, DBT, NBB, APEDA and have a CPCSEA-approved animal house along with well-defined IAEC, IBSC and IEC structures. These are probably one-of-the-kind, and literally state-of-the-art facilities to conduct research on Ayurveda. Top of the line equipment’s and globally trained workforce energizes the research operations on a daily basis. Job opportunity for the Drug Discovery & Development Division! Job Summary We are looking for a skilled and motivated Research Scientist with extensive hands-on experience in working with Zebrafish (Danio rerio). The candidate will be responsible for maintaining Zebrafish colonies, performing microinjection, and conducting experimental work related to developmental biology, toxicology, genetics, or disease modeling. This role requires strong technical expertise, precision, and a proactive approach to research. Job Responsibilities Perform microinjections (e.g., morpholino, CRISPR/Cas9, mRNA). Conduct developmental, toxicological, or behavioral assays. Handle dissection, imaging, and phenotype analysis of zebrafish embryos and larvae. Maintain accurate lab records and document experimental procedures. Collaborate with cross-functional research teams to drive projects forward. Prepare technical reports, presentations, and research summaries. Educational Experience And Requirements M.Sc./M.Tech/Ph.D. in Life Sciences, Biotechnology, Molecular Biology, or related field. Minimum 2 years of direct, hands-on experience working with Zebrafish. Strong understanding of Zebrafish as a model organism in genetics or developmental biology. Skilled in embryo handling, microinjection techniques, and zebrafish husbandry. Familiarity with microscopy and image analysis tools. Preferred Skills Experience with CRISPR/Cas9, morpholino knockdown, or transgenic zebrafish lines. Knowledge of toxicology assays or high-throughput screening using zebrafish. Ability to troubleshoot and optimize experimental workflows. Experience in scientific documentation and data analysis. Benefits Be part of a cutting-edge research team using Zebrafish to explore critical biological questions. Work in a collaborative and innovative environment with state-of-the-art facilities. Opportunities for professional development and impactful contributions. Patanjali Research Foundation is an equal opportunity employer and does not discriminate against any applicant because of race, colour, religion, gender, national origin, age and physical disability. How to Apply Write to jobs@patanjali.res.in, hr.prft@patanjanali.res.in with your detailed resume, cover letter and career aspirations. Mention Research Scientist-Zebrafish Model System in the subject field of your email. List three professional references other than your friends and family.

The Eco Toxicologist position based in Nagpur, India requires the candidate to hold a minimum of an M.Sc (or equivalent) in Toxicology, Ecotoxicology, Environmental Science, Fisheries, or Zoology. A PhD in the relevant field would be preferred. Additionally, familiarity and hands-on experience with Biodegradability, cell biology, fish studies & culture, and algal studies would be advantageous. The ideal candidate should have prior experience in conducting studies related to fish, algae, and Daphnia. Knowledge and experience in biodegradability are also desirable. Responsibilities include conducting desktop research, analyzing technical literature, reviewing, and summarizing scientific literature and pre-clinical study reports. The candidate will be required to interpret and apply existing information and data on chemicals to meet regulatory requirements. Additionally, the role involves coordinating with the laboratory, monitoring studies, and reviewing reports.,