Sandoz, a global leader in generic and biosimilar medicines, is inviting applications for the position of Specialist – QPPV in Telangana, India. This is a full-time opportunity within the Research & Development – Patient Safety function, supporting the Qualified Person for Pharmacovigilance (QPPV) office.
This role is ideal for professionals with experience in pharmacovigilance, clinical safety, deviation management, CAPA, audits, and global PV compliance, who are seeking to grow their career in a highly regulated, international environment.
Key Responsibilities – Specialist QPPV (Pharmacovigilance)
As a Specialist – QPPV at Sandoz, your responsibilities will include:
- Supporting deviation management, CAPA development, effectiveness checks, and closure across Patient Safety
- Acting as CAPA Coordinator in the GxQEM system
- Supporting pharmacovigilance inspections and audits, including CAPA tracking and follow-up
- Monitoring PV performance metrics, KPIs, and KQIs for internal teams and vendors
- Supporting the QPPV in meeting global legislative and regulatory requirements
- Reviewing emerging worldwide pharmacovigilance regulations and conducting impact assessments
- Supporting quality events and deviations as the business function owner
- Assisting with QPPV Office projects, documentation, and archival activities
- Supporting SOP management and quality management system (QMS) activities
- Identifying and escalating PV compliance risks based on data analysis and reports
Eligibility & Qualifications
Essential Requirements
- Minimum 2 years of experience in:
- Pharmacovigilance
- Clinical safety
- Drug development or related regulatory safety functions
- Strong knowledge of PV regulations, QPPV responsibilities, CAPA, and audits
- Excellent written and verbal communication skills
- Proven problem-solving, negotiation, and conflict-resolution abilities
- Strong planning, coordination, and computer literacy
- Ability to work independently under pressure with a results-driven mindset
Why Join Sandoz?
Sandoz is a pioneer in generic and biosimilar medicines, delivering over 900 million patient treatments across 100+ countries. Employees benefit from:
- Exposure to global pharmacovigilance systems
- Strong learning and career growth opportunities
- Collaborative and inclusive work culture
- Flexible and hybrid career options
- Meaningful work that improves global patient access to medicines
Job Location & Details
- Company: Sandoz
- Job Title: Specialist – QPPV
- Location: Telangana, India
- Functional Area: Research & Development (Patient Safety)
- Job Type: Full-time | Permanent
- Shift: General (No shift work)
Estimated Salary (India)
- ₹10,00,000 – ₹16,00,000 per annum
(Based on market standards for QPPV support and pharmacovigilance specialist roles in India)
How to Apply
