Company Name: Vivo Biotech Limited About our company Vivo Bio Tech Limited is a leading preclinical Contract Research Organization (CRO) based in Hyderabad, India. Vivo is OECD-GLP accredited, AAALACi certified pre-clinical testing facility. We specialize in offering comprehensive preclinical safety and analytical services across a wide range of industries, including pharmaceuticals, agrochemicals, industrial chemicals, medical devices, biopharmaceuticals, vaccines, herbal/nutraceuticals, and cosmetics. Position: Study Director - Toxicology Experience: 4+ years Location: Pregnapur, Hyderabad Job Description: 1. To act as a single point of control for conducting toxicity and efficacy studies (In-vivo and In-vitro) studies. 2. Responsibility for overall scientific conduct of the studies in compliance with the Principles of GLP, regulatory test guidelines and animal welfare guidelines like CCSEA. 3. Experience in conducting Acute, Repeated Dose, Reproductive, Inhalation, Immunogenicity and Neurotoxicity studies. 4. Hands on experience with various product lines like Pharma, Agrochemical, Industrial Chemicals, Microbial pesticides, Medical device, Biosimilars, Vaccines etc., 5. Experience in dosing different routes of administration in small & large animal models. 6. Functions will include study plan (and amendment) design and approval in accordance with internal procedures and where appropriate, in compliance with international regulations. 7. Effective co-ordination with cross functional team for proper planning, designing of the experiment, execution and reporting of the results. 8. Interpretation of the results, writing the discussion and conclusion for the final report. 9. To conduct and participate in the functional and cross functional meeting with respect to studies planned, ongoing or completed. 10. Familiar with the regulatory test guidelines (eg., OECD, ICH, ISO) and GLP Principles. 11. Knowledge in statistical analysis. 12. Liaise with the sponsor, auditors and consultants on study related materials. 13. Effective co-ordination with Quality Assurance & Management. 14. Sound communication with managerial skill. 15. Having proficiency in the various applications such as MS Word, Excel, PowerPoint etc., Thanks & Regards G NagaSravani - HR nagasravani.g@virinchi.com Show more Show less

We Are Hiring!!!! Company Name: VIVO BIO TECH Ltd. Job Position: Study Director - Analytical Chemistry Experience: 4-10 Years Location: Hyderabad Education: M.SC / M.Pharma / Ph.D in Analytical Chemistry, Pharmaceutical Sciences or related field CTC: As per company standards Role Description This is a full-time on-site role in Hyderabad for a Study Director - Analytical Chemistry at ViVo Biotech Ltd. The Study Director will be responsible for conducting laboratory experiments, research, toxicology studies, project management, and In Vivo testing. Thanks and Regards G NagaSravani nagasravani.g@virinchi.com

Job Title: Analytical Scientist – Phy-Chem Studies (Agrochemical & Pharma) Company Name: Vivo Biotech Ltd Location: Hyderabad Experience: 5 + Years Industry: Agrochemical / Pharmaceutical Research Job Description: We are seeking a detail-oriented and skilled Analytical Scientist with hands-on experience in conducting Phy-Chem and validation studies for agrochemicals and pharmaceutical compounds. The ideal candidate will have strong knowledge of global regulatory guidelines and be capable of preparing study-related documentation while maintaining audit readiness at all times. Key Responsibilities: · Conduct Physico-Chemical studies for agrochemical compounds in accordance with regulatory requirements. · Perform method validation studies for agrochemical products as per SANTEE/SANCO guidelines. · Execute validation studies for pharmaceutical compounds as per ICH guidelines. · Carry out dose formulation analysis to support toxicological and regulatory studies. · Prepare and maintain Standard Operating Procedures (SOPs) for newly initiated studies. · Develop study plans and compile final study reports as per relevant regulatory guidelines. · Ensure all studies are conducted in compliance with GLP, OECD, OPPTS, CIPAC, SANCO, and SANTEE guidelines. · Maintain effective communication with Quality Assurance (QA) personnel throughout the study lifecycle. · Utilize Microsoft Excel for accurate calculations, data analysis, and result interpretation. · Remain audit-ready at all times for sponsor audits, NGCMA inspections, or other regulatory reviews. Desired Candidate Profile: · Strong understanding of regulatory frameworks applicable to agrochemical and pharmaceutical studies. · Prior experience working in a GLP-compliant environment. · Excellent documentation and report writing skills. · Detail-oriented with good communication and coordination skills. · Flexible and proactive approach, especially regarding audit preparedness. Thanks and Regards G NagaSravani nagasravani.g@virinchi.com

Job Title: Study Director- Analytical Scientist - Phy-Chem Studies (Agrochemical & Pharma) Company Name: Vivo Biotech Ltd Location: Hyderabad Experience: 3 + Years CTC: 5Lpa - 3Lpa - 5.5Lpa Job Description: We are seeking a detail-oriented and skilled Analytical Scientist with hands-on experience in conducting Phy-Chem and validation studies for agrochemicals and pharmaceutical compounds. The ideal candidate will have strong knowledge of global regulatory guidelines and be capable of preparing study-related documentation while maintaining audit readiness at all times. Key Responsibilities: Conduct Physico-Chemical studies for agrochemical compounds in accordance with regulatory requirements. Perform method validation studies for agrochemical products as per SANTEE/SANCO guidelines. Execute validation studies for pharmaceutical compounds as per ICH guidelines. Carry out dose formulation analysis to support toxicological and regulatory studies. Prepare and maintain Standard Operating Procedures (SOPs) for newly initiated studies. Develop study plans and compile final study reports as per relevant regulatory guidelines. Ensure all studies are conducted in compliance with GLP, OECD, OPPTS, CIPAC, SANCO, and SANTEE guidelines. Maintain effective communication with Quality Assurance (QA) personnel throughout the study lifecycle. Utilize Microsoft Excel for accurate calculations, data analysis, and result interpretation. Remain audit-ready at all times for sponsor audits, NGCMA inspections, or other regulatory reviews. Desired Candidate Profile: Strong understanding of regulatory frameworks applicable to agrochemical and pharmaceutical studies. Prior experience working in a GLP-compliant environment. Excellent documentation and report writing skills. Detail-oriented with good communication and coordination skills. Flexible and proactive approach, especially regarding audit preparedness. Thanks & Regards G NagaSravani - HR nagasravani.g@virinchi.com

Job Title: Study Director (Toxicology, Analytical, Gen Tox) Company: Vivo Bio Tech Ltd Location: Hyderabad Experience: 4-10 Years Education: Postgraduate (Life Sciences/Pharmacology/Toxicology or related fields) Vivo Bio Tech Ltd is seeking experienced Study Directors to lead and manage preclinical studies in accordance with GLP and regulatory guidelines. The role involves planning, execution, monitoring, and reporting of toxicology, pharmacology, or biocompatibility studies. Requirements: Postgraduate degree in Life Sciences or related discipline. 4-10 years of relevant experience in preclinical/GLP studies. Strong understanding of regulatory guidelines and data integrity practices. Excellent analytical, communication, and project management skills. Thanks and Regards, G Naga Sravani HR-Recruiter nagasravani.g@virinchi.com