Greetings from Eurofins! We're excited to share an opportunity that aligns with your profile. We've sourced your resume from a portal and believe you'd be a great fit for our Group Leader position in the Department of Sub-chronic/Chronic at Eurofins Bangalore. Designation can be discussed later. Below are the details of the role: Location: Bangalore, Peenya Qualifications: Postgraduate in Life Sciences (M.Sc./M.V.Sc./Ph.D.) with specialization in Toxicology Job description: Execution/Planning/performing and reporting/ archiving of repeat dose toxicology studies. To Assist and work along with HOS/HOD in Planning, initiation and conduct studies Preparation of New SOPs, Protocols and Reports. Participate in GLP / AAALAC related activities and addressing the issues. To keep tab on resources, planning and milestones effectively Literature search / Provide guidance to staff. Ensuring all day-to-day activities by delegating relevant personal/s Define key resource needs against priorities and manage. To train junior staff and to bring them up to the expected proficiency levels for quality work as per GLP norms. Ensuring that all the instruments / equipments are maintained properly with timely maintenance and calibration / performance checks. Maintenance of animal house and relevant documents as per GLP and AAALAC norms. Planning for the effective usage of the available resource. Participate in GLP inspections and ensure relevant regulatory compliance guidelines. Ensure the preparation of calibration planner and its monitoring. Ensuring adaptation of proper safety precautions in the laboratory. Ensure in archiving of all study related materials. To provide technical review of all the procedures and SOPs in the Test Facility. To provide technical support to the staff in the conduct of GLP studies. Upgradation of the Animal Facility/Instruments as per the requirement. Validation of FOB Instruments and study with positive controls If you're interested, please review the full job description below and reply with your updated resume. How to Apply: Email: Sekhar.Sompalli@advinus.eurofinsasia.com WhatsApp: 8296695960 (calls restricted)

Job Description 5-7 years of experience in Preclinical CRO BD Business, Sales, Operational experience and tox study pricing knowledge. Should have knowledge about Indian Pharmaceutical testing requirements so that she / he can pitch our services at right stage. Exposure to preclinical and experience in managing Indian pharma companies as account manager. Self-driven, strong inclination to network and should be extrovert in nature Job requires frequent travel on monthly basis to client offices (minimum of 10 meetings at client office / month) Strongly believe in individual performance & Result oriented. Since Indian market we have sufficient connection, should have farming skills rather than hunting skills. To own target of INR 400 Mn as individual performer. Good presentation and communication skills, both verbal and written. If you're a fit, send your resume to Sekhar.Sompalli@advinus.eurofinsasia.com . Please share only relevant profiles, Mention the subject line - Business Development Bangalore

Role & responsibilities: Maintain instruments, equipment, and test systems (Fish, Daphnia, Alga, Earthworm, Honeybees, Silkworms) Assist in GLP/non-GLP ecotoxicology studies Write/revise SOPs and standardize new techniques Maintain logs, study records & raw data documentation Support study conduct, validation, reporting & QAU communication Archive study materials and ensure GLP compliance Preferred candidate profile: Maintenance of instrument and equipment in Ecotoxicology. Assisting in writing/Revision of SOPs. Standardization of new techniques. Maintenance and update of logbooks and record Maintenance of test systems- Fish, Daphnia, Alga, Earthworm, Honeybees, Silkworms Performance check of micro pipette and thermometers Other work as assigned by Head of Department

Job Title: Principal Scientist - (Study Director in Toxicology) Location: Bangalore Industry: Pre-clinical Contract Research Organization Job Type: Full-time About the Role: We are seeking an experienced Principal Scientist to lead our toxicology studies, designing, conducting, and reporting non-clinical safety studies (GLP and non-GLP) in support of drug development and regulatory submissions. This role demands strong scientific leadership, regulatory expertise, and cross-functional collaboration. Key Responsibilities: Design, conduct, and report non-clinical safety studies (GLP and non-GLP) for drug development and regulatory submissions. Provide scientific leadership and ensure regulatory compliance in toxicology studies. Collaborate with cross-functional teams to ensure study integrity and success. Requirements: Experience: 8-10 years of relevant experience in toxicology or a related field. Education: Ph.D. or Master's degree in Veterinary Sciences or Biosciences. Desirable Certifications: DABT Certification and FELASA certification. Skills: Expertise in repeat dose toxicity, teratology, and reproductive toxicity experimentation. Strong understanding of pharmaceutical R&D and agrochemical testing processes. Excellent team working and leadership skills. In-depth knowledge of GLP and regulatory guidelines. Strong scientific writing and communication skills. Ability to manage multiple projects and lead teams. Proficiency in data analysis and interpretation. Behavioral Competencies: Excellent communication and adaptability. Effective time management. Continuous learning and improvement. Structured work approach. What We Offer: Opportunity to work in a dynamic CRO environment. Collaborative team. Growth opportunities. If you are a motivated professional looking to lead in toxicology, apply now with your resume. How to Apply: Email: Sekhar.Sompalli@advinus.eurofinsasia.com

Job Title: Section Head (Toxicology)Location: Bangalore Industry: Pre-clinical Contract Research Organization Job Type: Full-time About the Role: We're seeking an experienced Section Head to lead our toxicology team, combining scientific expertise with strategic oversight. This dual-role position demands strong leadership, regulatory knowledge, and cross-functional collaboration to support drug development from discovery to late-stage clinical trials. Key Responsibilities: Design and manage toxicology studies. Mentor teams and shape toxicology strategy across programs. Collaborate with cross-functional teams to support drug development. Requirements: Experience: 12-15 years of relevant experience in toxicology or a related field. Education: Ph.D. or Master's degree in Veterinary Sciences or Biosciences. Desirable Certifications: DABT Certification and FELASA certification. Skills: Expertise in acute and repeat-dose toxicity studies. Strong understanding of pharmaceutical R&D and agrochemical testing processes. Proven cross-functional team collaboration. In-depth knowledge of GLP and global regulatory guidelines. Excellent scientific writing and communication skills. Strong team leadership and project management skills. High proficiency in data analysis and interpretation. Behavioral Competencies: Excellent communication and adaptability. Effective time management. Proven mentoring and team leadership. Experience integrating toxicology insights into clinical development. Ability to manage complex studies and cross-functional teams. What We Offer: Opportunity to lead in a dynamic CRO environment. Collaborative team. Growth opportunities. If you're a seasoned professional with expertise in toxicology and leadership, apply now with your resume. How to Apply: Email: Sekhar.Sompalli@advinus.eurofinsasia.com We look forward to hearing from you!