Regulatory Submissions jobs in Karnataka
Explore 17 current openings. Compare roles, companies, locations, and work options, then open any job to view the full details.
Current openings
Showing 20 jobsRegulatory Submission Specialist
GSKRegulatory Submission Specialist supports GSK’s regulatory submission activities, authoring, reviewing, and compiling dossiers for R&D and commercial projects. Works with submission teams, local contacts, and global …
Bengaluru, IndiaOn-siteFull-timeActiveRegulatory Specialist, Submission Coordination; SDE, LCM
GSKRegulatory Specialist, Submission Coordination works closely with global submission teams and local regulatory contacts to deliver end‑to‑end submissions on time and in compliance with regulatory guidelines and GSK …
Bengaluru, IndiaOn-siteFull-timeActiveRegulatory Submission Manager
GSKThe Regulatory Submission Manager leads end‑to‑end regulatory lifecycle submissions across multiple markets, ensuring compliance with GSK and global regulatory standards. The role coordinates cross‑functional teams, …
Bengaluru, Karnataka, IndiaHybridFull-timeActiveRegulatory Specialist, Submission Delivery Excellence
GSKRegulatory Specialist, Submission Delivery Excellence collaborates with global and local teams to deliver marketing applications, lifecycle maintenance submissions, and regulatory registration samples on time and in …
Bengaluru, IndiaHybridFull-timeActiveRegulatory Manager, Delivery, CMC RA
GSKRegulatory Affairs team at GSK leads CMC regulatory activities to support timely submissions and lifecycle management of vaccines. The Regulatory Manager coordinates complex CMC submissions, manages variation projects, …
Bengaluru,IndiaHybridFull-timeActiveClient Management Analyst
Wells FargoClient Management Analyst on Wells Fargo’s Sales Enablement team in Bengaluru. Builds and maintains research interaction workflows, automates data processes with VBA/SQL, and generates client‑centric analytics to …
Bengaluru,IndiaFull-timeActiveRegulatory Project Manager, New Registration CMC
GSKRegulatory Project Manager, New Registration CMC is a key role within GSK’s CMC RA group, responsible for leading the development and submission of complex CMC technical regulatory documents for new chemical entities, …
Bangalore, IndiaHybridFull-timeActiveRegulatory Affairs Consultant, Local Regulatory Affairs Operations
ParexelRegulatory Affairs team at Parexel focuses on post‑approval regulatory activities to ensure compliance and timely submissions worldwide. The Consultant manages variations, renewals, and dossier maintenance, partnering …
Bengaluru,IndiaRemoteFull-timeActiveClient Management Analyst
Wells FargoClient Management Analyst supports Sell Side Equity Advisory team, managing research interactions, maintaining databases, automating tasks, generating analysis, collaborating with stakeholders, ensuring timely …
Bengaluru, IndiaHybridFull-timeActiveRegulatory Affairs Consultant, Local Regulatory Affairs Operations
ParexelRegulatory Affairs Consultant on the Local Regulatory Affairs Operations team at Parexel, focused on managing post‑approval regulatory activities such as variations, renewals, and compliance across markets. The role …
Bengaluru,India,IndiaRemoteFull-timeActiveNonclinical Document Specialist
AstraZenecaNonclinical Submission group at AstraZeneca focuses on ensuring high‑quality nonclinical data for regulatory submissions. The specialist manages archive processes, coordinates data delivery, and edits submission …
Bangalore,IN,IndiaHybridFull-timeActiveRegulatory Affairs Associate, Local Regulatory Affairs Operations
ParexelRegulatory Affairs team at Parexel focuses on post‑approval regulatory activities to ensure therapies reach patients safely. The Associate manages variations, renewals, and compliance across country‑specific …
Bengaluru,India,IndiaRemoteFull-timeActiveRegulatory Affairs Global Regulations Specialist
PhilipsRegulatory Affairs Global Regulations Specialist responsible for monitoring global regulatory requirements, implementing strategy, coordinating compliance, managing submissions, building agency relationships, analyzing …
Bangalore, IndiaOn-siteFull-timeActiveRegulatory Affairs Associate I
AstraZenecaRegulatory Affairs Associate I at AstraZeneca supports drug development by managing regulatory submissions, document tracking, and interfacing with health authorities. The role involves preparing and executing simple …
Bangalore, IndiaHybridFull-timeActiveSenior Regulatory Affairs Associate
ParexelRegulatory Affairs Team at Parexel ensures compliance with European regulatory requirements for medicinal products. The Senior Associate validates and manages regulatory data, performs xEVMPD submissions via the EMA …
Bengaluru,IndiaRemoteFull-timeActiveRegulatory Specialist
GSKRegulatory Specialist, CMC Renewals team ensures Pharma and Vaccines products are safe, effective, and high quality. Author, compile, and check regulatory submissions for drug manufacturing and quality control. Works …
Bengaluru, IndiaOn-siteFull-timeActiveLead-Regulatory Reporting.CAD
Injaz - RBG - Emirati Deposits TeamLead-Regulatory Reporting on the Injaz – RBG – Emirati Deposits Team, driving the preparation and submission of regulatory reports for Mashreq UAE and its subsidiaries. The role ensures compliance with CBUAE and SCA …
Bengaluru, Karnataka, IndiaRemoteFull-timeActiveRegulatory Manager
CovanceRegulatory Affairs team ensures compliance and timely submissions for clinical studies. The Regulatory Manager oversees RA, IRB/EC, and third‑party submissions, coordinates timelines, and provides expert guidance on …
Bangalore,IndiaRemoteFull-timeActiveClient Onboarding Regulatory And Data Services - Director - Regulatory Change, Analytics & Strategy
Morgan StanleyWe’re seeking a Director to lead the Client Onboarding Regulatory & Data Services team in Bengaluru, India. The role focuses on product backlog grooming, value assessment, and backlog management for regulatory and data …
Bengaluru, IndiaOn-siteFull-timeActiveManager, Regulatory Affairs - India
Worldwide Clinical TrialsRegulatory Affairs department at Worldwide Clinical Trials, a global CRO, leads regulatory submissions and ethics committee coordination across EMEA, Asia Pacific and Latin America, ensuring compliance and supporting …
Virtual,India,IndiaRemoteFull-timeActive