Hiring Alert: MPharma Associate Scientist Job at Syngene – Apply Now!

Requisition ID: 55362

Posted: 03/19/2024

Job title: Associate Scientist/Sr. Associate Scientist

Job location: Bangalore

Job grade: 8-I/8-II

• 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

Working

• Conduct literature searches and prepare toxicological assessments of various raw materials/ingredients/API/ Pharmaceuticals used in consumer and OTC products.
• Preparation and reviewing of Nonclinical overview for CTD submission of dossier filing.
• Creation of Toxicology Profiles for INCI ingredients as well as residual chemicals.
• Conduct risk assessment for raw materials for cosmetic applications including Margin of safety calculations.
• To derive Health Based exposure limit (PDE/OEL/DNEL/ADI) for Pharmaceuticals/ cosmetics/ nutraceuticals/ agrochemicals/ botanicals.
• To provide evidence of efficacy and safety (preclinical and clinical) as per regulatory requirements.
• Preparation of Safety Data sheet in compliance with GHS.
• Scientific literature search-To extract, analyze and collate toxicology data from various clinical/toxicology/efficacy related databases like TOXNET, HSDB, PubMed, Medline, ScienceDirect etc.
• To evaluate quality of different toxicity studies (such as systemic toxicity, genotoxicity, skin/eye irritation, sensitization, carcinogenicity, reproductive and developmental toxicity, toxicokinetic studies) as per OECD/ ICH /FDA/ISO guidelines.
• To prepare research reports/ dossiers according to the international regulatory guidelines.

• Excellence
• Integrity
• Professionalism

Educational Qualification: M.Pharma/M.Sc/MVSc

Experience: 3-6 years