Sandoz Hiring Pharmacovigilance Specialist QPPV
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Education
- Experience Requirements
- Key Skills & Competencies
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Who is eligible to apply for the Specialist QPPV role?
- Is this role suitable for freshers?
- Is the role regulatory-facing?
- What type of company is Sandoz?
- Where is the job located?
- Is this a permanent position?
- Summary Table
Specialist QPPV – M.Pharm/B.Pharm – Sandoz India Vacancy
Sandoz India hiring Specialist QPPV in Telangana. Apply now for 1 vacancy. Eligible M.Pharm, B.Pharm, Pharm.D candidates.
Sandoz has opened an important career opportunity within its Patient Safety and Pharmacovigilance leadership framework with the hiring of a Specialist – QPPV (Qualified Person for Pharmacovigilance) in India. This role sits at the intersection of regulatory compliance, quality systems, and global pharmacovigilance operations, making it highly relevant for professionals aiming to build long-term careers in drug safety, regulatory affairs, and clinical risk management.
As part of the Research & Development function, the Specialist QPPV role supports critical safety governance activities that ensure medicines remain compliant, safe, and accessible across global markets. The position is based at the Sandoz Telangana site and offers exposure to global audits, inspections, deviation management, and regulatory intelligence. For professionals with experience in pharmacovigilance quality systems and CAPA management, this is a high-impact opportunity within a globally respected pharmaceutical organization.
Company Overview
Sandoz is a global leader in generic and biosimilar medicines, playing a foundational role in expanding patient access to affordable, high-quality treatments. In 2024 alone, Sandoz delivered more than 900 million patient treatments across over 100 countries, reinforcing its position as one of the most trusted names in the pharmaceutical industry.
The company operates across development, manufacturing, and commercialization of generics and biosimilars, with strong investments in innovation, digital quality systems, and regulatory excellence. Sandoz maintains a robust pharmacovigilance and patient safety ecosystem aligned with global regulatory authorities including EMA, FDA, MHRA, and other international health agencies.
Job Role & Responsibilities
The Specialist – QPPV role is a critical support function within the QPPV Office and Patient Safety organization. The position focuses on pharmacovigilance quality systems, deviation management, CAPA oversight, audit readiness, and regulatory compliance support.
Key Responsibilities
- Support the development, implementation, and management of pharmacovigilance deviations, quality events, and associated Corrective and Preventive Actions (CAPAs).
- Act as a CAPA coordinator within the GxQEM system, ensuring timely documentation, tracking, closure, and effectiveness checks.
- Provide operational support for pharmacovigilance inspections and audits, including preparation, response coordination, and post-inspection CAPA management.
- Support QPPV oversight activities to ensure compliance with global legislative and regulatory pharmacovigilance requirements.
- Monitor and analyze patient safety performance metrics, KPIs, and Key Quality Indicators (KQIs) for internal teams and external vendors.
- Support regulatory intelligence activities, including review of emerging global pharmacovigilance regulations and assessment of operational impact.
- Serve as the business function representative for allocated deviations and quality events across the Patient Safety organization.
- Identify potential compliance risks through metrics analysis and escalate issues proactively to relevant stakeholders.
- Support development, review, and maintenance of Patient Safety SOPs, work instructions, and controlled documentation.
- Assist with coordination, documentation control, and archival activities within the QPPV Office.
- Contribute to cross-functional projects related to pharmacovigilance quality management systems and continuous improvement initiatives.
This role demands strong attention to detail, regulatory awareness, and the ability to operate effectively under inspection and compliance-driven environments.
Eligibility / Qualifications
Required Education
Candidates should hold a relevant life sciences or pharmacy qualification. Accepted courses include:
B.Pharmacy, M.Pharmacy, Pharm.D, MSc Clinical Research, MSc Pharmacovigilance, MSc Life Sciences, MSc Biotechnology, MSc Biochemistry
Experience Requirements
- Minimum of 2 years of experience in drug development, clinical safety, pharmacovigilance, or closely related pharmaceutical development functions.
- Hands-on exposure to pharmacovigilance quality systems, deviation management, CAPA processes, audits, or inspections is strongly preferred.
Key Skills & Competencies
- Strong understanding of global pharmacovigilance regulations and quality management systems.
- Experience working with electronic quality management systems (eQMS), preferably GxQEM or equivalent platforms.
- Effective written and verbal communication skills for regulatory documentation and cross-functional coordination.
- Sound negotiation, conflict resolution, and problem-solving abilities.
- Results-driven mindset with the ability to work independently and manage multiple priorities under pressure.
- Strong planning, coordination, documentation, and computer skills.
Location & Salary
- Job Location: Telangana, India (Sandoz site)
- Employment Type: Full-time, Regular
Application Process
Interested and eligible candidates must apply online through the official Sandoz careers portal.
Apply Link: https://www.sandoz.com/careers/career-search/job-details/REQ-10024484/specialist-qppv/
Frequently Asked Questions (FAQs)
Who is eligible to apply for the Specialist QPPV role?
Candidates with B.Pharm, M.Pharm, Pharm.D, or relevant life sciences postgraduate degrees and at least two years of experience in pharmacovigilance or clinical safety are eligible.
Is this role suitable for freshers?
No. This position requires a minimum of two years of relevant industry experience.
Is the role regulatory-facing?
Yes. The role supports inspections, audits, and compliance activities aligned with global regulatory authorities.
What type of company is Sandoz?
Sandoz is a global pharmaceutical leader specializing in generic and biosimilar medicines, operating in over 100 countries.
Where is the job located?
The role is based in Telangana, India, at the Sandoz site.
Is this a permanent position?
Yes. This is a full-time, regular employment role.
Summary Table
| Company | Sandoz |
|---|---|
| Vacancies | 1 |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, MSc Clinical Research, MSc Pharmacovigilance, MSc Life Sciences |
| Experience | Minimum 2 years in Pharmacovigilance / Clinical Safety |
To apply for this job please visit www.sandoz.com.
