Freshers Pharm D Jobs | Drug Safety Associate Jobs
Kickstart your career in Pharmacovigilance with one of the fastest-growing pharma service providers in India. GSS Pharma Pvt. Ltd., Bangalore is now hiring Drug Safety Associates — an excellent opportunity for freshers and early-career professionals to enter the global pharmaceutical safety domain. With hands-on exposure to case processing, literature screening, XEVMPD/EVWEB updates, and regulatory documentation, this opening is ideal for candidates seeking Freshers Pharm D Jobs | Drug Safety Associate Jobs in a dynamic, innovation-driven environment.
GSS Pharma Pvt. Ltd., Bangalore
Drug Safety Associate (Pharmacovigilance)
Location: Bangalore
Vacancies: 4
Experience: 0 – 3 years (PV experience preferred)
Qualification: Pharm D / M.Pharm
Pay: Performance‐based compensation
Company Overview:
GSS Pharma Pvt. Ltd. is an expanding player in the global pharmaceutical services space, dedicated to delivering regulatory, safety and business operations support across international markets. Our Bangalore facility is focused on building a dynamic, innovation-driven environment for pharmacovigilance and global regulatory excellence.
Role Description:
We are seeking a detail-oriented Drug Safety Associate to support our pharmacovigilance operations. In this role you will be responsible for processing Individual Case Safety Reports (ICSRs), conducting literature screening, maintaining XEVMPD and EVWEB updates (including SmPC/PIL documentation), review of SmPC and PIL versus reference products, tracking safety signals and compliance with SOPs and relevant regulations. You will have the opportunity to gain exposure to international safety frameworks, regulatory systems and global operations while growing your career in pharmacovigilance.
Key Responsibilities:
- Process Individual Case Safety Reports (ICSRs) accurately and timely.
- Conduct literature screening activities and assess abstracts/articles for validity and further safety database processing.
- Maintain XEVMPD and EVWEB updates, including Summary of Product Characteristics (SmPC/SmPC), Patient Information Leaflet (PIL) inserts and updates.
- Review SmPC and PIL documents in comparison with reference products.
- Monitor safety signals and track updates on products in the client portfolio.
- Ensure strict adherence to standard operating procedures (SOPs) and regulatory requirements.
If you are eager to build your career in pharmacovigilance, work with global regulatory and business operations, and thrive in an innovation-focused setting, we would love to hear from you.
