Evalueserve India
Location
Bangalore | India
Job description
Evalueserve is a global leader in delivering innovative and sustainable solutions to a diverse range of clients, including over 30% of Fortune 500 companies. With presence in more than 45 countries across five continents, we excel in leveraging stateof-the-art technology, artificial intelligence, and unparalleled subject matter expertise to elevate our clients' business impact and strategic decision-making. We have 4,500+ talented professionals operating across 45 countries, including India, China, Chile, Romania, the US, and Canada. Our global network also extends to emerging markets such as Colombia, the Middle East, and the rest of Asia-Pacific. Recognized by Great Place to Work® in India, Chile, Romania, the US, and the UK in 2022, we offer a dynamic, growth-oriented, and open culture that prioritizes flexible work-life balance, diverse and inclusive teams, and equal opportunities for all.
Key Responsibilities: Prepare comprehensive Common Technical Document (CTD) dossiers in compliance with international regulations and marketing submission requirements. Develop and review reports on Health Based Exposure Limits (HBELs) such as (PDE/ OEL/ ADI) for various chemicals. Conduct scientific literature searches to gather, analyze, and compile relevant scientific data from diverse clinical and non-clinical safety, and efficacy databases. Evaluate the quality, produce data summaries, and draw conclusions for various toxicological endpoints such as systemic toxicity, genotoxicity, skin/eye irritation, sensitization, carcinogenicity, reproductive toxicity, developmental toxicity, and toxicokinetics, in accordance with guidelines/ guidance established by OECD, ICH, and EPA. Review and author hazard or safety assessments for various chemical products such as pharmaceuticals, cosmetics, nutraceuticals, agrochemicals, botanicals, and biomedical devices. Draft environmental and ecotoxicity assessments pertaining to chemicals, specifically addressing factors like persistence, bioaccumulation, and toxicity Skills Required: Preparation of HBELs as per regulatory requirements. Demonstrate expertise in writing and submitting hazard or safety documentation in compliance with various regulations such as EU, EPA, ICH, or FDA. Familiar with a range of toxicology, pharmacology, clinical, and regulatory databases, as well as their search strategies, for the purpose of identifying high-quality data. Demonstrates a comprehensive understanding of diverse toxicological studies and their principles in accordance with OECD guidelines. Excellent interpersonal skills and effective written and verbal communication abilities. Proficient in completing tasks within assigned areas of responsibility with accuracy and timeliness. Exhibits attentive and active listening skills. Demonstrates strong teamwork skills and logical reasoning. Displays the ability to identify proactive approaches to contribute towards the firm's goals and mission. Open to challenging existing practices by introducing innovative work methodologies. M.Sc, M. Pharmor Ph.D in Toxicology/Regulatory Toxicology. A minimum of 5+ years of professional experience in the chemical, consumer product, or pharmaceutical industry. ERT or DABT certification preferred Location: Bangalore & Gurgaon JOB APPLICANT PRIVACY NOTICE: By applying for a job application for any position at Evalueserve, you acknowledge and agree that Evalueserve will collate and process your personal data for the recruitment purpose. The personal and sensitive personal data will be processed (which includes, in particular collecting, storing, utilizing, processing, sharing or transferring) by Evalueserve strictly on a need-to-know basis and retained until required for legitimate business purposes. For more details, please visit Evalueserve’ s website and privacy policy on the homepage. To Know More: Follow us on: Read about us: Interested applicants can share resume - [email protected]Job tags
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