Manager - Registration Management
Abbott
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This role on the market
24 open registration roles across 13 companies are on ApplySarthi right now, most of them in Mumbai (1).
- Registration Referral SpecialistJobgether
- Munich Open Day RegistrationPtc
- Registration Lead, Product Success - FTC until Jan 2028Relx
- Operations Senior Specialist II - Capital Market RegistrationJPMorgan
- Transfer Agency - Registration Services, Associate 2Statestreet
What registration roles keep asking for: Accounting (17%), Stakeholder management (17%) — counted across their open postings here.
Abbott has 5,392 open roles listed here.
- SW Test Engineer IImumbai
- Safety Specialist
- Application and Project Portfolio Lead
- CRM Senior Data Analyst
- Talent Acquisition Coordinator (2-year contract)
Counted across 14 company job boards, updated as roles open and close.
Preparing for this interview
Interviews for registration roles keep coming back to Accounting, Stakeholder management. Practise those questions before you sit with Abbott.
Questions you are likely to be asked
- Why do you want to join Abbott?
- What is your experience with Stakeholder management? Tell me one thing you learned the hard way.
- Tell me about yourself, and why this role is the right next step.
- Tell me about a problem you solved at work that you are proud of.
- Tell me about a time you disagreed with your manager. What happened?
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Practise the Manager - Registration Management at Abbott interview free →JOB DESCRIPTION: Role Purpose Provide strategic and operational leadership for Regulatory Information Management (RIMs) to ensure accurate, compliant, and timely management of global regulatory data, product lifecycle activities, and inspection readiness. Key Responsibilities Lead and develop a high‑performing RIMs team to deliver seamless day‑to‑day regulatory operations. Oversee creation and maintenance of regulatory applications for NPIs, safety variations, and lifecycle activities. Provide subject‑matter expertise and operational support for regulatory activities managed within centralized RIMs systems. Manage workflows for timely delivery of critical regulatory reports (e.g., Status, Product Quality, WWMAS) supporting supply, manufacturing, PV inspections, and governance. Own XeVMPD submissions and ongoing maintenance of registered product data. Ensure accuracy, integrity, and completeness of registered product and master data across global markets (LATAM, METAP, APAC, EU, India, and others). Maintain and update SOPs and Work Instructions for assigned workstreams, ensuring continuous audit and inspection readiness. Support regulatory audits and health authority inspections through RIMs expertise, data extraction, and documentation. Lead User Acceptance Testing (UAT) and related testing for new features, system enhancements, or major RIMs implementations. Drive continuous improvement, data quality excellence, and compliance with global regulatory requirements. Manage team performance, capability building, and career development. Required Expertise Strong knowledge of global regulatory regulations and guidelines. Hands‑on experience with industry‑standard RIMs tools and regulatory systems. Proven people leadership and stakeholder management capability. The base pay for this position is N/A In specific locations, the pay range may vary from the range posted. JOB FAMILY: Regulatory Operations DIVISION: EPD Established Pharma LOCATION: India > Mumbai : Mumbai Development Center - EPD ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Not specified MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Not Applicable
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Listed on workday · posted 2026-10-13. ApplySarthi collects openings and links to application pages; the role is advertised by Abbott, not by us.