Specialist -QPPV Job at Sandoz India | Top Pharma & Jobs | Apply Now
Looking to advance your career in Pharma Jobs or PV Jobs in India? Sandoz, a global leader in generics and biosimilars, is hiring a Specialist – QPPV in Telangana, India. This exciting Pharma Job in India offers the opportunity to support quality, compliance, and patient safety within a collaborative and innovation-driven environment. If you have experience in drug development, clinical safety, or pharmacovigilance, Sandoz provides the perfect platform to grow your career while making a global healthcare impact.
Job Details:
- Job Title: Specialist – QPPV
- Job ID: REQ-10024484
- Functional Area: Research & Development
- Employment Type: Regular, Full-Time
About the Company:
Sandoz is a global leader in generic and biosimilar medicines, offering exceptional opportunities for professionals seeking Pharma Jobs in India. With operations in over 100 countries and a focus on innovation and sustainability, Sandoz empowers its employees to help millions access high-quality healthcare worldwide. In 2024 alone, the company delivered over 900 million patient treatments, reinforcing its commitment to affordable and accessible medicine. Careers in Pharma are promising here.
Job Description For Pharma Jobs
The Specialist – QPPV role supports the development, management, and implementation of deviations, CAPAs, and effectiveness checks across the Patient Safety (PS) organization. You will work cross-functionally to ensure compliance and quality excellence while contributing to the QPPV Office in inspection readiness, audit operations, and quality management systems. This Pharma role demands meticulous attention to detail.
Key Responsibilities in PV Jobs:
- Support development, management, and implementation of deviations, CAPAs, and effectiveness checks across the PS organization.
- Coordinate inspection and audit operations, including CAPA tracking and management.
- Serve as CAPA coordinator within the GxQEM system.
- Oversee PV performance through metrics, KPIs, and KQIs for PS and key vendors. Working in Pharma Jobs requires dedication to performance excellence.
- Assist QPPV in ensuring global compliance with legislative requirements.
- Review emerging worldwide regulations and assess their impact.
- Collaborate on deviation management processes and documentation.
- Provide QPPV Office project support, including SOP management.
- Identify, analyze, and escalate compliance or risk issues promptly.
- Maintain documentation and archival activities within the QPPV Office.
Qualifications and Skills For Pharma Jobs:
- Minimum 2 years’ experience in drug development, clinical safety, or pharmacovigilance. Finding Pharma Jobs with this qualification broadens your opportunities.
- Excellent negotiation, conflict resolution, and communication skills.
- Proactive and transparent work ethic with strong accountability.
- Exceptional planning, coordination, and computer skills.
Why Join This Company:
At Sandoz, your contributions make a difference in providing affordable, high-quality medicines across the globe. With ongoing investments, acquisitions, and innovation, Sandoz fosters a culture of collaboration, growth, and inclusivity. Joining Sandoz means being part of a global team that’s redefining the future of healthcare through Pharma Jobs and PV Jobs that truly make an impact.
