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Associate - Toxicology

CLINCHOICE PRIVATE LIMITED

Location
Mumbai, IN
Employment
Full-time
Posted
3d ago
General ProfessionalClinical Scientific RegulatoryCommunication Storytelling

About this role

<p style="line-height: 1;"><strong><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Job Description</span></strong><br><strong><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Job Title: Associate – Regulatory Toxicology</span></strong><br><strong><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Employment Type: Full-time</span></strong><br><strong><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Location: Mumbai, India</span></strong></p> <p style="line-height: 1;"><strong><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">About ClinChoice</span></strong><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in </span><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, </span><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by </span><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">accelerating clinical trials with data-driven insights, delivering the best strategies for product registration, </span><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">and enhancing patient safety through real-world and clinical analysis.</span></p> <p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Our global delivery network has expanded to centers and satellite offices in the United States, Mexico, </span><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">the United Kingdom, Armenia, China, Japan, India, and the Philippines to help our customers maintain </span><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">regulatory compliance locally and globally.</span></p> <p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">We have forged future-defining partnerships with industry bodies and technology companies to develop </span><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">cutting-edge solutions that deliver our expertise with quality and precision.</span></p> <p style="line-height: 1;"><strong><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Primary Responsibilities:</span></strong><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Conduct literature searches and prepare toxicological assessments of various raw </span><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">materials/ingredients used in consumer and OTC products.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Create Raw Material Toxicology Profiles for INCI ingredients as well as residual chemicals.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Conduct risk assessments for raw materials used in cosmetic applications, including Margin </span><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">of Safety and California Proposition 65 calculations.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Draft Full Safety Assessments as required by the European Cosmetics Directive.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Draft safety assessments for impurities and degradants based on requirements.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Draft Full Safety Assessments, including recommendations for the approval of formulas.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Complete all assigned training within the specified timelines.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Participate in Process Improvement Initiatives to maintain the Quality and Compliance </span><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">score.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Escalate any issues encountered during daily activities to the Team Lead on a daily basis.</span></p> <p style="line-height: 1;"><strong><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Candidate Profile:</span></strong><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Minimum of 2–4 years of experience in the pharmaceutical industry as a Regulatory Toxicologist.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Master's degree in Toxicology or Veterinary Pharmacology.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Good verbal and written communication and presentation skills in English.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Should be proactive and initiative-driven.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Should be solution-centric in approach.</span></p> <p> </p>

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