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Regulatory Submissions jobs
Explore 66 current openings for Regulatory Submissions jobs. Compare roles, employers, locations, and work options on Chuno.
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- RPCurrent opening
Senior 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-timeReview matching role → - HCurrent opening
Submission 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 plat…
Chennai,IN,IndiaHybridFull-timeReview matching role → - ACurrent opening
IS 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 acceptanc…
Hyderabad, IndiaOn-siteFull-timeReview matching role → - JCurrent opening
Principal Regulatory Medical Writer
jobgetherRegulatory Medical Writing team drives creation of high-quality regulatory and clinical documentation for innovative healthcare products. The Principal writer leads development of complex submissions, mentors junior w…
IndiaRemoteFull-timeReview matching role → - BSCurrent opening
Submission Document Manager
Bristol-Myers Squibb CompanyRegulatory Operations at Bristol Myers Squibb leads the development and delivery of clinical and regulatory submission documentation for global health authority filings. The Submission Document Manager coordinates cro…
Hyderabad, Telangana, IndiaOn-siteFull-timeReview matching role → - ACurrent opening
Sr Associate Software Engineer – Regulatory Structured Submission
AmgenAutomate regulatory content via VBA on GxP platform. Create and enhance VBA macros and user interfaces. Implement robust error handling and debugging. Document code and processes for maintainability. Collaborate with…
Hyderabad, IndiaOn-siteFull-timeReview matching role → - SPCurrent opening
Regulatory Affairs Executive
Sun Pharma IndustriesRegulatory Affairs team in Sun Pharma R&D ensures product registrations across global health authorities. The Executive reviews dossiers, compiles eCTD submissions, and leads responses to agency queries while coordina…
Baroda, IndiaOn-siteFull-timeReview matching role → - GCurrent opening
Regulatory Submission Lead, SDE LCM
GSKRegulatory Submission Lead at GSK works within the Regulatory Affairs team to independently drive global drug registration dossiers, coordinating with CMC, Clinical, and Non‑clinical functions. The role authors, revie…
Bengaluru, IndiaHybridFull-timeReview matching role → - PCurrent opening
Senior Regulatory Affairs Associate
ParexelRegulatory Affairs Team at Parexel supports global regulatory lifecycle management across EU, US and international markets. The Senior Associate develops regulatory strategies, prepares submission packages, manages po…
Bengaluru,IndiaRemoteFull-timeReview matching role → - ACurrent opening
Senior Regulatory Services Associate
AccentureLife Sciences R&D vertical at Accenture delivers regulatory services for biopharma clients, ensuring compliance across research, clinical trials, and patient solutions. The Senior Regulatory Services Associate coordin…
Bengaluru, IndiaOn-siteFull-timeReview matching role → - ACurrent opening
Senior Associate IS Analyst
AmgenAutomate regulatory content on GxP platform using VBA, design MS Office interfaces, implement robust error handling, document code, test and validate changes, collaborate with regulatory experts, provide technical val…
Hyderabad, IndiaOn-siteFull-timeReview matching role → - ACurrent opening
Associate IS Business Systems Analyst
AmgenJoin Amgen’s mission to serve patients. As an Associate IS Business Systems Analyst, you’ll lead Scrum events for the Regulatory Structured Submissions Team, enhancing communication, aligning with program goals, and d…
Hyderabad, IndiaOn-siteFull-timeReview matching role → - ACurrent opening
Assistant Manager, Regulatory Affairs
AmnealRegulatory Affairs team at Amneal drives global compliance for product development. The Assistant Manager leads dossier compilation, eCTD submissions, and DMF processes, ensuring audit readiness and regulatory intelli…
IndiaOn-siteFull-timeReview matching role → - MCurrent opening
Manager, Regulatory Compliance
MastercardGlobal Regulatory Team at Mastercard drives compliance across the Asia Pacific region, ensuring regulatory obligations are met for payments products and services. The Manager provides key regulatory compliance support…
Mumbai,,IndiaOn-siteFull-timeReview matching role → - ACurrent opening
Regulatory Senior QA
AccoliteRegulatory Reporting QA team at Accolite ensures compliance of financial reporting solutions with global standards. The Senior QA Engineer leads end‑to‑end testing of regulatory reporting pipelines, validating data ac…
Gurugram, Haryana, IndiaOn-siteFull-timeReview matching role → - ADCurrent opening
Regulatory Affairs Intern
AVEVA DRUG DELIVERY SYSTEMS INCRegulatory Affairs team at AVEVA Drug Delivery Systems supports product registrations by preparing and submitting regulatory dossiers to health authorities. The intern tracks global regulatory updates, maintains filin…
Hyderabad, Telangana, INOn-siteInternshipReview matching role → - ACurrent opening
Veeva Submission SME
AtosAtos, a global leader in secure digital solutions, seeks a Veeva Submission SME for its Chennai team. The role focuses on publishing regulatory submissions via Veeva Vault RIM, ensuring compliance with eCTD standards…
Chennai,IN,IndiaOn-siteFull-timeReview matching role → - APCurrent opening
Senior Executive, Regulatory Operations & Compliance
Advanz PharmaRegulatory Publishing team at Advanz Pharma ensures accurate and compliant regulatory data submissions. The Senior Executive drives XEVMPD/IDMP submission execution, supports system implementation, and improves data m…
Andheri, Mumbai, IndiaHybridFull-timeReview matching role → - ACurrent opening
Senior Associate Regulatory Affairs
AmgenROOTS2 team within Amgen's Regulatory Affairs CMC group drives regulatory strategy and submission execution for biologics and device products. The Senior Associate leads annual and product renewal submissions, coordin…
Hyderabad,India,IndiaOn-siteFull-timeReview matching role → - APCurrent opening
Manager, Regulatory Affairs
Azurity Pharmaceuticals - IndiaRegulatory Affairs team at Azurity Pharmaceuticals ensures compliance and strategic regulatory support for innovative drug products. The Manager leads cross‑functional project teams, drives regulatory strategies, prep…
Hyderabad,IN,IndiaOn-siteFull-timeReview matching role →
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