 Teva Pharmaceuticals is committed to diversity and equal employment opportunities. We ensure that employment decisions are made without regard to race, age, gender, disability, or any other legally protected status. We encourage candidates who require accommodations to apply and will provide support throughout the recruitment process.
Experience Required:
3-4 years in pharmacovigilance, including experience in Individual Case Safety Report (ICSR) processing and literature review.
Qualification:
Any life sciences/pharmaceutical/healthcare professional graduate (B. Pharmacy, M. Pharmacy, Pharm D, BDS).
Solid understanding of pharmacovigilance concepts, regulations, and procedures
Advanced proficiency in Microsoft Office platforms
Minimum of 3-4 years of experience in pharmacovigilance including literature review process in ICSR
Experience in patient safety/pharmacovigilance: solid knowledge in pharmacovigilance concepts, regulations, and procedures.
Advanced knowledge of Microsoft Office platforms.
Flexible to adapt to shifting team priorities.
Excellent communication skills including written, verbal, and non-verbal.
Excellent Interpersonal and people skills. Good analytical skills and problem-solving skills.
Key Responsibilities:
As a Pharmacovigilance Professional at Teva Pharmaceuticals, you will:
Conduct workshops, training sessions, and hands-on mentorship for new hires.
Act as a subject matter expert, providing guidance on case processing and pharmacovigilance updates.
Participate in activities of literature review. Design and implement comprehensive literature search strategies on specific products. Knowledge of database: Embase, Medline, Pubmed, Ovid, etc.
Assess the impact of regulatory changes on the current process.
Contribute to simplification of processes.
Knowledge and expertise in Teva portfolio.
Support pharmacovigilance teams like case processing, training teams, quality assurance, audits and inspections etc.
Act as a consultant or SPOC for various case related activities and maintain knowledge repository of the process updates/ regulatory changes on real time.
Effective communications to be maintained with internal (related departments and units) & external (partners, authorities, vendors) stake holders in order to run the process as transparent as possible.
Ensure that quality data is analyzed for any trending and to prepare team for process stabilization.
Ensure regulatory compliance by following internal reporting key performance indicators for the unit are met.
Independent operations and self-promoted initiatives are expected to interpret and make valuable decisions in ever changing and dynamic requirements from regulators.
Being part of transitions to the team and to other teams and certification of the teams on the same.
Conduct various interactive activities like workshops, trainings, sessions to educate the team on the existing and on predicted error trends for process improvements.
Provide the analytical support for the peers and managers in investigations and analysis of various trends as a part of audits, and inspections.
Mentoring the new hires with case processing knowledge transfer, evaluating their progress close to perfection during their initial phases of learning curves.
Perform other tasks assigned by the direct manager.
Location: Bangalore, India (560052)
Position: Pharmacovigilance Professional
How to Apply
Ready to take the next step in your career? Apply online for the Pharmacovigilance Professional role at Teva Pharmaceuticals via the link below:
Apply Here
Alternatively, you can send your updated resume directly to ankita.sonawane@teva.co.in.
