hirly

Abbott

Manager - Registration Management

India > Mumbai : Mumbai Development Center - EPD

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Abbott first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.6M live jobs from 210,000+ employers in 200+ countries.

Tailor my resume for this job →

Apply from your AI assistant

Connect hirly to Claude or ChatGPT and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending.

Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.

hirly's read of this role

Seniority
Lead / management
Country
IN
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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

Original posting on Abbott's site ↗

Listed on hirly, a job board. hirly is not the employer: Abbott is hiring for this role.

Browse similar roles

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job