vacancies

The QPPV support team is headed by the QPPV (EEA & UK QPPV) and is an expert interface for regulatory and scientific requirements and build the interface between Local/Regional safety regulatory environment and Global product Teams, both in development and post-marketing.

Bachelors degree with clinical Data Management experience, including managing multiple clinical projects and serving as the primary sponsor contact.

Responsible for leading and overseeing local pharmacovigilance activities, including adverse event case processing, safety reporting to Health Authorities, customer complaint handling, regulatory compliance, data quality, and stakeholder collaboration across clinical development and post-marketing activities.

Bachelors degree in Biological Science (biology, microbiology, Molecular Biology) or technical discipline at minimum.

Experience in Pharmacovigilance and Medical Information regulatory requirements, systems, and processes

Matriculation or its equivalent examination. Applicant should possess minimum qualification of Diploma in Pharmacy from recognized University registered under Pharmacy Act, 1948.

The candidate should have a two-year Diploma in Pharmacy (D-Pharma) (ALLOPATHIC) from any institute approved by the Pharmacy Council of India.

MSc / MPharm from recognised University / Institute. experience in research/teaching/industry and established reputation of having made conspicuous seminal contribution to knowledge in Pharmaceutical and allied areas. Central Instrumentation Facility, Centre of Excellence, NIPER-Guwahati