Safety Reporting Business Application Specialist - Hyderabad
Johnson & Johnson · Healthcare & Pharma
- Hyderabad, Andhra Pradesh, India
- On-site
- Posted yesterday
- Apply by 8 Oct
About the job
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com .
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Product Safety
Job Sub Function:
Pharmacovigilance
Job Category:
Scientific/Technology
All Job Posting Locations:
Hyderabad, Andhra Pradesh, India
Job Description:
Position Title:
Safety Reporting Business Application Specialist - Hyderabad
Position Summary
The main purpose of the Safety Reporting Business Application Specialist position is:
To provide operational pharmacovigilance expertise and business systems support for global safety reporting activities and systems. The role will combine a strong understanding of day-to-day safety reporting requirements with the systems knowledge needed to support Global Safety Reporting leadership and activities across the safety reporting software development lifecycle. The role will act as a bridge between safety reporting business users, the Business Application Owner, development teams, and external vendors. It will translate regulatory and operational needs into clear business and functional requirements for system configuration.
Key responsibilities may include:
Major Duties & Responsibilities
Major responsibilities are listed in order of approximate percentage of time. The percentages may vary according to project and operational priorities.
Tasks / Duties / Responsibilities
Safety Reporting Operations & Business Analysis - 55%
Business Application Support & System Lifecycle Management - 35%
Maintain clear business and functional documentation to support system reliability, knowledge transfer within Global Safety Reporting, audit readiness, and business continuity.
10%
Quality, Documentation & Training - 10%
Perform other duties that are consistent with the role and may be assigned according to business, regulatory, operational, or project needs.
Key Working Relationships
Internal
Global Safety Reporting, Global Case Management, Global Development, Information Technology, Quality, Data Privacy, Information Security, Procurement, Legal, Regulatory, and other system or process stakeholders.
External
eSUSAR distribution system vendor, outsourcing vendor teams, software developers, technical support teams, implementation partners, and other service providers.
Decision Making Authority
Decision Making Authority
Required Qualifications
Required Minimum Education:
Bachelor’s degree in life sciences, pharmacy, computer science, information systems, engineering, data science, or a related discipline, or equivalent relevant experience.
Required Years of Related Experience:
Previous pharmaceutical industry, clinical, pharmacovigilance, or safety systems experience, typically demonstrated by a minimum of 8+ years of relevant experience. Experience must include practical knowledge of safety reporting operations and involvement in technical system support, system implementation, database integration, or business analysis.
Required Knowledge, Skills and Abilities:
Pharmacovigilance & Regulatory Expertise
Business Applications, Systems & Data.
Business Analysis & Communication
Preferred Qualifications
Preferred Minimum Education:
Bachelor’s degree or higher in a relevant life science or technical discipline.
Preferred Area of Study:
Life sciences, pharmacy, pharmacovigilance, computer science, information systems, engineering, data science, or a related field.
Preferred Related Industry Experience:
Experience with pharmacovigilance technology platforms, eSUSAR distribution systems, regulated system implementation, data migration, or digital transformation projects.
Preferred Knowledge, Skills and Abilities:
Hands-on experience with SQL or another query language; application programming interfaces; structured data formats; integration or middleware platforms; cloud-based applications; reporting or analytics tools; Agile delivery; and regulated system lifecycle or validation practices.
Key Working Relationships
Travel on the Job:
Yes
Percentage Traveled:
<5%
Type of Travel Required:
Domestic and international, as needed
People Management Experience:
No
Required Years of People Management Experience:
N/A
Supervisory Responsibility:
Direct reports: 0; Indirect reports: 0
Required Skills:
Preferred Skills:
Clinical Operations, Coaching, Critical Thinking, Cross-Functional Collaboration, Health Intelligence, Performance Measurement, Pharmacovigilance, Process Optimization, Quality Control (QC), Quality Management Systems (QMS), Regulatory Affairs Management, Report Writing, Root Cause Analysis (RCA), Safety Investigations, Safety-Oriented, Serious Adverse Event Reporting, Technologically Savvy