Invivo Pharmacology Scientist

Job Title: Invivo Pharmacology Scientist Job Location: Bangalore About Syngene: Syngene ( is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene’ s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time JOB PURPOSE (Briefly describe the objectives of the job): Responsible for executing the assigned in vivo efficacy studies in metabolic disorder therapeutic area. KEY RESPONSIBILITIES: Responsible to conduct assigned research projects including experiments with utilizing current concepts and recognized standard techniques. Responsible to set up the experimental designs, analysis of data and concluding from the progress. Record laboratory observations information in lab notebooks, database and document the experimental designs. Responsible for data analysis, perform calculations for the result of the experiment. Summarize the research and communicate result of research to the supervisor. EDUCATIONAL QUALIFICATION: M.Pharm Pharmacology M.V.Sc Pharmacology/Pathology M.Sc. Neuroscience/Biochemistry/Biotechnology WORK EXPERIENCE: 1 - 6 years of Industrial experience TECHNICAL /FUNCTIONAL SKILLS: Hands-on experience in execution of CNS disease models which includes psychiatric disorders such as anxiety, depression, PTSD etc., and neurological conditions like Alzheimer’s disease, Parkinson’s disease, cerebral ischemia and epilepsy. Hands-on experience in animal behavioral observation, quantification of animal behavior, experience in stereotaxic surgery, microdialysis, cannulation techniques, immunohistochemistry and ELISA. Will work independently or in association with senior scientists and other associates in the design and execution of in-vivo efficacy experiments in the relevant therapeutic area. Experience in animals handling (rodents and non rodents) such as dosing by various routes, bleeding by various routes, injections by various routes and surgical modalities which includes cannulation etc… Associate to provide technical, analysis and reporting outcomes of research for projects in relevant therapeutic area. Organizational skills and the ability to work in a highly collaborative environment are required. BEHAVIORAL/MANAGERIAL SKILLS: Good communication skills Excellent interpersonal skills. Good team player Strong documentation Skills. Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodation for qualified individuals with disabilities.