Pharmacovigilance Specialist ICSR Openings at Johnson & Johnson
- Pharmacovigilance Specialist ICSR Openings for Life Sciences in Hyderabad
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Additional Expectations
- Eligibility / Qualifications
- Required Education
- Required Experience
- Preferred Qualifications
- Behavioral Competencies
- Location & Salary
- Application Process
- FAQs
- Who can apply for the Pharmacovigilance Specialist ICSR role?
- Is PV case-processing experience mandatory?
- What safety systems are preferred?
- Is this a hybrid role?
- What qualifications are needed?
- Does this job involve global collaboration?
- Summary Table
Pharmacovigilance Specialist ICSR Openings for Life Sciences in Hyderabad
Apply for Pharmacovigilance Specialist ICSR positions in Hyderabad. Openings for Life Sciences, Pharmacy, Nursing graduates with 5–8 years experience.
Johnson & Johnson is hiring experienced pharmacovigilance professionals for its ICSR function in Hyderabad. This role is designed for specialists who can strengthen global case management through advanced, technology-enabled processes. Candidates with strong scientific expertise and hands-on PV operations experience will find this a high-impact opportunity to shape how safety data is captured, processed, and delivered across global healthcare systems.
Company Overview
Johnson & Johnson is a global healthcare leader operating across Innovative Medicine and MedTech. The company focuses on transforming patient outcomes through evidence-based solutions, advanced therapeutics, and digital innovation. Its pharmacovigilance division supports global safety operations, ensuring that adverse event data is accurate, compliant, and aligned with regulatory expectations. The Hyderabad site plays a key role in case management modernization, contributing to innovation across safety systems and technology platforms.
Job Role & Responsibilities
The Specialist, Pharmacovigilance, ICSR role is positioned within Product Safety and supports capability development for global case management. The focus is on creating efficient, compliant, and data-driven workflows.
Core Responsibilities
- Lead the design, deployment, and improvement of ICSR tools using automation and digital technologies
- Partner with global case management teams to ensure operational readiness for new capabilities
- Support governance, training, and performance monitoring for system reliability and inspection readiness
- Apply pharmacovigilance expertise to assess data accuracy and workflow alignment
- Identify process gaps and execute corrective and preventive actions
- Contribute to case management operations by reviewing capability-linked activities
- Develop case-testing scenarios, test scripts, and validation steps for system behavior and data integrity
Additional Expectations
- Maintain high levels of compliance and documentation accuracy
- Work collaboratively across global teams and time zones
- Manage responsibilities independently with strong problem-solving ability
- Demonstrate consistent professionalism and quality-focused behavior
Eligibility / Qualifications
Required Education
Accepted qualifications include:
B.Sc, M.Sc, B.Pharm, M.Pharm, Pharm.D, Nursing, MBBS, Biomedical Sciences, Biotechnology, Biochemistry, Life Sciences, Clinical Research.
Required Experience
- 5–8 years of experience in pharmacovigilance, ICSR, or regulated safety operations
- Strong knowledge of seriousness, causality, MedDRA coding, expectedness, case intake, processing, and reporting
- Experience with ICSR process design, improvements, or automation initiatives
- Hands-on experience in writing or executing test scripts for safety systems
Preferred Qualifications
- Experience with Argus, ArisGlobal LifeSphere, or similar safety databases
- Exposure to AI, automation, or GenAI-driven PV projects
- Familiarity with quality systems, QMS, RCA, or safety investigations
- Ability to work effectively in dynamic and evolving environments
Behavioral Competencies
Professionals in this role must demonstrate:
- Independent decision-making
- Strong analytical reasoning
- Effective communication across cross-regional teams
- Attention to detail with a quality-first mindset
- Collaboration, empathy, and adaptability
Location & Salary
- Location: Hyderabad, Andhra Pradesh, India
- Work Pattern: Hybrid
- Salary: Competitive and aligned with industry standards, based on experience and technical capability
Application Process
Candidates can submit their application through the Johnson & Johnson career portal.
Apply here: https://www.careers.jnj.com/en/jobs/r-045354/specialist-pharmacovigilance-icsr-hyderabad/?source=LinkedIn
Complete the online application, attach your resume, and ensure your experience in ICSR, case management, and PV systems is clearly highlighted.
FAQs
Who can apply for the Pharmacovigilance Specialist ICSR role?
Professionals with 5–8 years of PV experience and a strong understanding of ICSR processes.
Is PV case-processing experience mandatory?
Yes. Deep knowledge of intake, processing, reporting, and safety regulations is required.
What safety systems are preferred?
Argus, ArisGlobal LifeSphere, or similar global safety databases.
Is this a hybrid role?
Yes. The position follows a hybrid work pattern.
What qualifications are needed?
Degrees in Life Sciences, Pharmacy, Medicine, or Nursing.
Does this job involve global collaboration?
Yes. The role collaborates with cross-regional teams to enhance case management capabilities.
Summary Table
| Category | Details |
|---|---|
| Company | Johnson & Johnson, Hyderabad |
| Vacancies | Specialist, Pharmacovigilance, ICSR |
| Required Education | B.Sc, M.Sc, B.Pharm, M.Pharm, Pharm.D, Nursing, MBBS, Biotechnology, Biochemistry, Biomedical Sciences, Life Sciences, Clinical Research |
| Experience | 5–8 years in pharmacovigilance or ICSR operations |
To apply for this job please visit www.careers.jnj.com.
