Job Title: Analytical Scientist - Phy-Chem Studies (Agrochemical & Pharma) Company Name: Vivo Biotech Ltd Location: Hyderabad Experience: 3+ Years CTC: 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 Description: We are seeking a detail-oriented and skilled Analytical Scientist (Five Batch Analysis) 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. Act as Study Director for Five Batch Analysis studies in accordance with CRO and GLP regulatory requirements. Develop study plans, protocols, and schedules for analytical method validation and sample analysis. Review raw data, analytical reports, and ensure accurate documentation for regulatory submissions. 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. Key Skills: Study Direction & GLP Compliance Five Batch Analysis & Regulatory Submissions Analytical Method Development & Validation HPLC, UPLC, LC-MS/MS Expertise Data Integrity & Quality Assurance Client and Sponsor Interaction Leadership & Team Mentoring Qualifications & Experience: Masters/PhD in Analytical Chemistry / Pharmaceutical Chemistry / Life Sciences or related discipline. 4-8 years of experience in Analytical R&D, QC, or CRO environment with exposure to GLP studies. Hands-on experience with HPLC, UPLC, LC-MS/MS, and other advanced analytical techniques. Prior experience as a Study Director for GLP studies, specifically Five Batch Analysis (mandatory). Regards NagaSravani G nagasravani.g@virinchi.com
Job Title : Veterinarian Preclinical (CRO & GLP) Location: Pregnapur, Hyderabad Experience : 1-3 years of experience in preclinical CRO Reports To : Head Preclinical Research / Study Director / TFM Job Summary: We are seeking a qualified and experienced Veterinarian to support preclinical research programs within a GLP-compliant Contract Research Organization environment. The veterinarian will be responsible for the care, welfare, and regulatory compliance of laboratory animals used in safety, pharmacology, and toxicology studies, ensuring adherence to OECD GLP guidelines and sponsor requirements. Key Responsibilities: Animal Care & Welfare Oversee the health and welfare of laboratory animals (rodents, rabbits, dogs, non-human primates, etc., depending on facility scope). Conduct daily health observations, physical examinations, and maintain detailed medical records. Provide preventive and therapeutic veterinary care in accordance with GLP guidelines. Research Support Work closely with study directors, toxicologists, and animal facility staff to support preclinical studies. Participate in study design discussions to ensure compliance with GLP and animal welfare regulations. Administer test compounds (oral, intravenous, subcutaneous, etc.) and collect biological samples (blood, urine, tissues). Support surgical and anesthesia procedures where required. Regulatory Compliance Assist in preparing and reviewing study protocols, SOPs, and reports for GLP compliance. Support inspections and audits from regulatory authorities and accreditation bodies. Documentation Maintain accurate and complete veterinary records in compliance with GLP principles. Prepare health status reports, necropsy reports, and incident documentation. Qualifications Education: Bachelors in Veterinary Science & Animal Husbandry (B.V.Sc & A.H.), with registration from Veterinary Council of India (VCI). Master’s degree in Veterinary Regards, Anusha Patnaik|Assistant Manager|HRD Vivo Bio Tech Ltd., Vivo Bio Science Park, Pregnapur Village, Gajwel Mandal. Siddipet District, Telangana, India. Email: anusha.p@vivobio.com | hrd@vivobio.com Website : www.vivobio.com