13 Safety Assessment Jobs

As a Site Supervisor, your primary responsibility will be to maintain project administration in a correct and timely manner. This includes tasks such as ordering materials and equipment, handling necessary permits, and ensuring that construction human resource objectives are met by selecting, orienting, and training employees. You will also be responsible for assessing safety and finance goals, as well as managing sub-contractors by locating, evaluating, and selecting contractors. - Order materials and equipment required for the project - Take care of necessary permits and approvals - Ensure construction human resource objectives are met by selecting, orienting, and training employees - Asse...

Date: 12 Dec 2025 Location: IN Division: Discovery Services Job Description Job Title : Medical Monitor Department : Medical & Regulatory Affairs Operating Unit: Translational and Clinical Research Job Location : Bengaluru, Karnataka About Syngene: Syngene ( www.syngeneintl.com ) 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, i...

As a Regulatory Toxicology & Pharmacology professional at our company in Kolkata, your role will involve the following: - Clear understanding of Regulatory Toxicology & Pharmacology principles with robust domain knowledge - Good understanding of OECD guidelines Safety Guidelines - Familiarity with risk assessment, Hazard assessment, Exposure assessment & Safety assessment - Knowledge of various Toxicology/ Pharmacology/ clinical/ Regulatory databases - Knowledge of dose calculation & conversions - Capability of interpretation of results and analysis of key toxicity data Qualifications required for this role are: - M. Pharm in Pharmacy - MS/M.Sc(Science) in Chemistry,

Xenish Remedies is looking for Safety Assessment to join our team Roles and Responsibility Conduct thorough safety assessments to identify potential hazards and risks. Develop and implement effective safety protocols and procedures. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Perform regular audits and inspections to ensure adherence to safety standards. Provide training and guidance on safety procedures to employees. Investigate incidents and accidents to determine root causes and implement preventive measures. Job Requirements Strong knowledge of safety regulations and standards. Excellent analytical and problem-solving skills. Ability to work...

As a critical member of the team, your primary responsibility will be to drive the design, execution, and interpretation of preclinical studies to support the discovery and development of novel therapeutics for neurological disorders. Your deep expertise in neuroscience, pharmacology, and translational science will play a key role in advancing drug candidates, including biologics and gene therapies, from early discovery through IND-enabling studies. **Key Responsibilities:** - Lead preclinical strategy and execution for neuroscience drug discovery programs. - Design and oversee in vivo and in vitro studies to evaluate pharmacodynamics, efficacy, and safety. - Guide target validation, biomark...

Your future role Take on a new challenge and apply your rigorous and structured expertise in a new cutting-edge field. Youll work alongside dedicated, resilient, and collaborative teammates. You'll ensure the safety and reliability of our projects and products by conducting thorough assessments. Day-to-day, youll work closely with teams across the business (Engineering, Project Management, Quality Control), deploy safety assessment processes and tools and much more. Youll specifically take care of delivering safety assessment reports, presenting assessment results to various stakeholders, and managing safety findings logs, but also support safety reviews and independent assessments as needed...

Role Overview: As a critical member of the team, you will be responsible for driving the design, execution, and interpretation of preclinical studies to support the discovery and development of novel therapeutics for neurological disorders. Your expertise in neuroscience, pharmacology, and translational science will be instrumental in advancing drug candidates, including biologics and gene therapies, from early discovery through IND-enabling studies. Key Responsibilities: - Lead preclinical strategy and execution for neuroscience drug discovery programs. - Design and oversee in vivo and in vitro studies to evaluate pharmacodynamics, efficacy, and safety. - Guide target validation, biomarker ...

You will be working as a Site Supervisor with the primary responsibility of maintaining project administration in a correct and timely manner. This will involve tasks such as ordering materials and equipment, handling necessary permits, and ensuring that construction human resource objectives are met by selecting, orienting, and training employees. Additionally, you will be responsible for assessing safety and finance goals, as well as managing sub-contractors by locating, evaluating, and selecting contractors. Key Responsibilities: - Order materials and equipment required for the project - Take care of necessary permits and approvals - Ensure construction human resource objectives are met b...

Provide comprehensive contract research services in drug discovery, preclinical, and early development stages. Conduct regulatory toxicology studies for safety assessment to support drug development pipelines. Perform DMPK (Drug Metabolism and Pharmacokinetics) studies to evaluate ADME (Absorption, Distribution, Metabolism, and Excretion) profiles of drug candidates. Deliver Analytical R&D services including method development, validation, and stability studies for early-stage drug substances. Support API CDMO (Active Pharmaceutical Ingredient Contract Development and Manufacturing Organization) operations, focusing on manufacturing drug substances for toxicology and early clinical studies. ...

As a Regulatory Toxicology & Pharmacology professional in Kolkata, you will be expected to have a clear understanding of Regulatory Toxicology & Pharmacology principles with robust domain knowledge. Additionally, you should possess a good understanding of OECD guidelines Safety Guidelines and be familiar with risk assessment, Hazard assessment, Exposure assessment & Safety assessment. Your role will also require knowledge of various Toxicology/ Pharmacology/ clinical/ Regulatory databases and dose calculation & conversions. With 2-3 years of experience, you should have the capability of interpretation of results and analysis of key toxicity data. Qualifications required for this position inc...

As a Medicinal Chemistry leader at Alembic, you will be at the forefront of driving the next wave of therapeutic innovation. Your role will involve shaping the future of drug discovery from India and bridging into the U.S. biotech ecosystem. Based in Hyderabad Genome Valley, you will work full-time and report to the Head of Drug Discovery at Alembic. You will be tasked with spearheading small-molecule and peptide drug discovery efforts, shaping and executing innovative strategies that drive programs from target identification to nominating clinical candidates. Alembic is seeking a visionary and accomplished leader with a track record of advancing compounds from early discovery to IND-enablin...

Job Summary: This dual customer/product focused position serves as the senior technical liaison between OEMs and represents our customers during new product development programs. Applying Cummins products to customer vehicles requires the development of technical specifications, implementing new design configurations, and delivering high performance, low-cost equipment and system solutions integrated with customers products in a variety of applications. Integrating high quality and optimized customer solutions requires the interaction with sales and marketing teams. Key Responsibilities: Obtains input and negotiates with Subject Matter Experts and Value Package Introduction (VPI) Teams and d...

look to you for: Planning and executing Independent Safety Assessment activities for assigned projects Applying and contributing to the continuous improvement of safety assessment processes and tools Delivering clear and comprehensive safety assessment reports Presenting results and managing communications with project teams and external entities Supporting the Independent Safety Assessment director or Safety Assessment lead in capturing assessment requests Contributing to the success of internal/external audits on process compliance Master Degree in Engineering or a similar technical field Experience in the railway safety domain or extensive experience in the railway domain with a focus on ...