Global Regulatory Compliance Expert
1 week ago
Regulatory Affairs SpecialistThis role involves working on formulation regulatory affairs for peptide products or injectables. The responsibilities include drafting controlled correspondences, preparing regulatory submission strategies, compiling CTD sections, and reviewing technical inputs during the product life cycle.Hands-on expertise of handling peptide or injectable products.Well-versed with regulatory guidelines.Candidates should have relevant experience and share their CVs along with details such as total experience, current salary, handling experience of peptide regulatory or not, notice period, and willingness to work in Bangalore onsite.What You Will DoIn this role, you will be responsible for managing the regulatory affairs for peptide products and injectables. This includes developing strategies for regulatory submissions, preparing controlled correspondences, and reviewing technical inputs during the product life cycle.Key ResponsibilitiesDrafting controlled correspondences for regulatory submissionsPreparing regulatory submission strategies for peptide products and injectablesCompiling CTD sections for regulatory submissionsReviewing technical inputs during the product life cycleRequirementsHands-on expertise of handling peptide or injectable productsWell-versed with regulatory guidelinesCandidates should have relevant experience and be willing to work in Bangalore onsite. We are looking for individuals who are detail-oriented, proactive, and able to work effectively in a team environment.
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Bangalore, Karnataka, India ExxonMobil Full timeAbout us At ExxonMobil our vision is to lead in energy innovations that advance modern living and a net-zero future As one of the world s largest publicly traded energy and chemical companies we are powered by a unique and diverse workforce fueled by the pride in what we do and what we stand for The success of our Upstream Product Solutions and Low Carbon...
