Regulatory Submissions jobs
Explore 46 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 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 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-timeActiveEditorial Submission Advisor
Springer NaturePublishing Performance and Intelligence Group (PP&I) Centre of Excellence at Springer Nature drives continuous improvement in journal publishing. The Editorial Submission Advisor screens transferred manuscripts, …
Pune,IndiaOn-siteFull-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-timeActiveRA CMC Senior Submission Coordinator
NovartisThe RA CMC Senior Submission Coordinator will independently manage complex CMC submissions, ensuring regulatory compliance and timely delivery. Responsibilities include QC and DA checks, eCTD documentation, database …
Hyderabad, IndiaOn-siteFull-timeActiveRegulatory Affairs Specialist
MedtronicRegulatory Affairs Specialist at Medtronic drives compliance for design, development, and regulatory submissions. Leads coordination of document packages for global submissions, renewals, and inspections. Recommends …
Nanakramguda, Hyderabad, IndiaHybridFull-timeActiveRegulatory Submission Operations Specialist
Regeneron PharmaceuticalsRegulatory Submission Operations team at Regeneron India ensures timely, compliant MHRA Clinical Trial Authorization submissions via the IRAS portal. The Specialist completes and uploads CTA applications, manages …
Hyderabad,IN,IndiaHybridFull-timeActiveGDO Submission Document Senior Specialist
Bristol-Myers Squibb CompanyGDO Submission Document team ensures clinical submission deliverables meet quality and regulatory standards. The Senior Specialist partners with the Submissions Document Manager, drives development of protocol-related …
Hyderabad,IN,IndiaOn-siteFull-timeActiveRegulatory Submissions Associate Manager
CovanceRegulatory Submissions team at Covance ensures timely and compliant regulatory authority, IRB/EC, and third‑body submissions across APAC clinical trials. The Associate Manager oversees submission strategy, timeline …
Remote India,INHybridFull-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-timeActiveGlobal Regulatory Submission Manager
NovartisNovartis’ Regulatory Affairs team in Hyderabad drives cross‑functional projects to plan, compile and dispatch worldwide regulatory submissions. The role manages multiple global eCTD and non‑eCTD dossiers (NDA/BLA/IND, …
Hyderabad,IN,IndiaOn-siteFull-timeActiveIS Organizational Effectiveness Manager – Regulatory Structured Submission
AmgenFacilitate Scrum events for Regulatory Structured Submissions Team, enhance communication, manage risks, drive continuous improvement, adapt SAFe principles, lead product delivery, prioritize backlog, define acceptance …
Hyderabad, IndiaOn-siteFull-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 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-timeActiveGDO Submission Document Senior Specialist
Bristol-Myers Squibb CompanyGDO Submission Document team at Bristol Myers Squibb focuses on preparing and quality‑checking clinical submission deliverables for global drug development. The Senior Specialist partners with the Submissions Document …
Hyderabad,TS,IndiaHybridFull-timeActiveSubmission Specialist
HavasSubmission Specialist at Havas Creative, the go‑to expert on client regulatory submission processes. The role partners with project management, account, editorial, and copy teams to ensure flawless submissions to …
Chennai,IN,IndiaHybridFull-timeActiveGlobal Regulatory Submission Manager
NovartisEnsures controlled documentation, record retention, and compliance with global regulatory agencies. Manages complex submission projects, develops strategy, supports global systems, resolves issues creatively, and …
Hyderabad, Telangana, IndiaOn-siteFull-timeActiveR&D Submission & Document Services Lead
SanofiHead of R&D Submission & Document Services at Sanofi’s Hyderabad Hub, driving regulatory excellence by leading a diverse team of submission and document specialists. The role focuses on ensuring timely, high‑quality …
Hyderabad,IndiaFull-timeActiveSenior Manager Regulatory Submission Operations
Regeneron PharmaceuticalsRegulatory Submission Operations team at Regeneron drives the end‑to‑end delivery of clinical trial authorisation submissions via the IRAS portal. The Senior Manager leads a team of specialists, oversees quality, RFI …
Hyderabad, IndiaHybridFull-timeActive