Occupational Toxicologist

In this role youwill…Provides expert toxicology review ofGSK Safety Data Sheets (SDS) for GSK drug substances,intermediates, mixtures, products etc. Interfaces with SDS authorsto ensure timely and accurate development /updates;Provides expert toxicology assessments(human health hazard assessments) and guidance for GSK products andprocess materials across global span of GSK, including developmentof Health based exposure limits (HBELs): Occupational exposurelimits (OELs), Permitted Daily Exposure (PDE) Limits for variousmodalities (small molecules, peptides, biologics, oligonucleotides,etc)Provides worldwide training and support intoxicologically related topics, establishes and maintains processesto enable effective communication and education of keystakeholders, maintains the global EHS toxicologydatabase;Support to worker safety testingprograms at external toxicology labs relevant for hazardcharacterization for new product and to support chemicalregistration data requirementsContribute toprojects to ensure regulatory compliance; authoring and/orreviewing reports, protocols, guidelines and standard operatingprocedures (SOPs) and ensuring harmonized approaches with regard tothe toxicological assessments;Monitorscientific developments and conduct desktop research includingliterature searches, and critically evaluate and summarisescientific information and governmentregulations.Maintain toxicological expertiserelevant to nonclinical safety of drugs, occupational health, andproduct quality risk, i.e. keeps up to date with the scientificliterature and regulatory guidance, attends and contributes torelevant professional/scientific meetings, and publishes in peerreviewed journals, if appropriateWhyyou?BasicQualificationsWe are lookingfor professionals with these required skills to achieve ourgoals:Significant experience in toxicologyfieldBSc degree or equivalent intoxicology/pharmacology or relatedResearchskills with literature searches, toxicology databases, regulatorydatabases and computational toolsProjectplanning, tracking and management skills to ensure actions andcommitments are delivered to planCImindedAmbitious, proactive andmotivatedPreferredQualificationsIf you have thefollowing characteristics, it would be aplus:Experience in regulatory toxicology,gained in pharmaceutical / biopharmaceutical, chemical, or relatedproduct manufacturingMasters degree orequivalent in toxicologyProfessionalQualification/Certifications (e.g DABT, ERT orsimilar).An understanding of GloballyHarmonized System (GHS) for classification and labelling ofchemicals and the EU Classification, Labelling and Packaging (CLP)regulation and other relevant globalregulationsKnowledge of global chemicalregulations and hazardassessments INT