Apply for Baxter Hiring for Spec PV Job Gurgaon for pharmacy, nursing and life sciences candidates with pharmacovigilance experience.
Pharmacovigilance professionals looking to build their careers in global drug safety and patient safety operations now have an excellent opportunity with Baxter. The company is hiring for the position of Spec, PV in Gurgaon, Haryana.
This latest Pharmacovigilance job is ideal for candidates with medical, pharmacy, nursing, or life sciences backgrounds who have experience in adverse event processing, Individual Case Safety Reports (ICSRs), MedDRA coding, and safety database operations. Candidates interested in working with global patient safety teams and regulatory compliance systems are encouraged to apply.
The role is part of Baxter’s Global Patient Safety (GPS) division and offers excellent exposure to international pharmacovigilance operations, patient safety processes, and healthcare compliance standards.
Job Details
| Job Information | Details |
|---|---|
| Job Role | Spec, PV |
| Company | Baxter |
| Department | Global Patient Safety (GPS) |
| Location | Gurgaon, Haryana |
| Job Type | Full-Time |
| Industry | Pharmaceutical & Healthcare |
| Application Deadline | May 29, 2026 |
| Job Requisition ID | JR – 200888 |
| Experience Preferred | Pharmacovigilance / Regulatory / Safety Experience |
| Qualification | Nursing, Pharmacy, Science Degree or Equivalent |
About the Company
Baxter is a globally recognized healthcare organization dedicated to improving patient care and advancing healthcare delivery worldwide. Since 1931, the company has focused on its mission to save and sustain lives through innovative healthcare solutions, medical technologies, and patient-centered services.
Baxter operates globally and supports healthcare systems through advanced pharmaceutical products, medical devices, and patient safety operations.
Job Overview
The Spec, PV role is part of the Safety Operations team within Global Patient Safety (GPS). The selected candidate will support adverse event processing, Individual Case Safety Report (ICSR) management, medical review activities, and pharmacovigilance database operations.
Professionals in this role will ensure timely and accurate processing of adverse event reports while maintaining compliance with global pharmacovigilance regulations and quality standards.
Key Responsibilities
Adverse Event Processing
- Process adverse event reports from multiple source types
- Review and perform full data entry of adverse event reports
- Determine seriousness, expectedness, causality, and event resolution
- Ensure correct suspect drug selection within the safety database
Safety Database and Coding Activities
- Code medical terms using MedDRA dictionaries
- Ensure accurate data entry and coding within the Pharmacovigilance Safety System
- Maintain quality and compliance standards for safety reports
- Support case cleanup activities for aggregate reporting preparation
Medical Writing and Narrative Preparation
- Write narratives summarizing medical information for ICSRs
- Review clinical and safety-related documentation
- Ensure all required safety information is captured accurately
Case Follow-Up and Investigation
- Generate and track follow-up queries
- Coordinate with reporters and local affiliates for case investigation
- Gather additional medical information for incomplete reports
- Perform quality checks when required
Required Qualifications
Candidates applying for this Pharmacovigilance position should possess:
- Degree in Nursing
- Pharmacy Degree
- Science Degree
- Equivalent healthcare or life sciences qualification
Relevant educational backgrounds may include:
- B.Pharm
- M.Pharm
- Pharm.D
- BSc Life Sciences
- MSc Life Sciences
- Nursing
Preferred Experience
Candidates with the following experience will be preferred:
- Pharmacovigilance operations
- Regulatory affairs
- Safety database management
- Hospital or patient care experience
- Adverse event processing
- Medical review and coding activities
Preferred experience level:
- 2–3 Years in healthcare, patient care, safety, or pharmaceutical operations
Required Skills
Applicants should demonstrate strong knowledge and expertise in:
- Pharmacovigilance safety systems
- Individual Case Safety Reports (ICSRs)
- MedDRA coding
- Adverse event processing
- Global safety regulations
- Medical terminology
- Clinical and medical knowledge
- Regulatory compliance standards
Additional Skills
Candidates should also possess:
- Strong written and verbal communication skills
- Attention to detail
- Ability to work independently
- Time management and multitasking skills
- Team collaboration abilities
- Capability to work under strict deadlines
Why Join Baxter?
Working with Baxter provides excellent opportunities for career growth in global patient safety and healthcare operations.
Benefits of Joining
- Exposure to international pharmacovigilance projects
- Experience with global safety regulations
- Opportunity to work with advanced safety systems
- Career growth in drug safety and regulatory operations
- Collaborative and purpose-driven work culture
- Professional learning and development opportunities
Career Growth Opportunities
Candidates joining as Spec, PV can build careers in:
- Pharmacovigilance Operations
- Drug Safety Associate Roles
- Safety Scientist Positions
- Medical Review and Coding
- Regulatory Affairs
- Signal Detection and Risk Management
- Global Patient Safety Operations
Equal Opportunity Employer
Baxter is an equal opportunity employer committed to diversity, inclusion, and workplace equality. The company considers qualified applicants without discrimination based on gender, disability, religion, age, race, or other legally protected categories.
Baxter also supports workplace accommodations for individuals requiring assistance during the recruitment and interview process.
How to Apply
Interested and eligible candidates should apply online before the application deadline.
Applicants are advised to prepare an updated resume highlighting:
- Pharmacovigilance experience
- Adverse event processing expertise
- Safety database and MedDRA knowledge
- Regulatory compliance experience
- Communication and medical writing skills
For more latest Pharmacovigilance, Drug Safety, Clinical Research, Regulatory Affairs, Pharma, and Healthcare job updates, visit latestpharmajobs.in regularly.
Conclusion
The Spec, PV opening at Baxter is an excellent opportunity for healthcare and life sciences professionals seeking career growth in global patient safety and pharmacovigilance operations. Candidates with ICSR processing, MedDRA coding, and safety operations experience should apply quickly before the deadline.