Teva Pharmaceuticals Hiring Pharmacovigilance Associates

Teva Pharmaceuticals Hiring Pharmacovigilance Associates

Are you passionate about contributing to global healthcare and making a positive impact on people’s lives? Teva Pharmaceuticals is looking for skilled Pharmacovigilance Associates to join their team in Bangalore, India. Discover more about this exciting opportunity, including responsibilities, qualifications, and how to apply.

About Teva Pharmaceuticals

Teva Pharmaceuticals is a global leader in generic medicines, committed to making good health more accessible and affordable worldwide. With a presence in nearly 60 countries and a diverse workforce, Teva is dedicated to producing essential medicines and improving healthcare outcomes for millions of people.

Job Overview: Pharmacovigilance Associate II

• Location: Bangalore, India, 560052
• Company: Teva Pharmaceuticals
• Job ID: 57966

Responsibilities:

1. Participate in activities of literature review. Design and implement comprehensive literature search strategies on specific products. Knowledge of database: Embase, Medline, Pubmed, Ovid, etc.
2. Assess the impact of regulatory changes on the current process.
3. Contribute to simplification of processes.
4. Knowledge and expertise in Teva portfolio.
5. Support pharmacovigilance teams like case processing, trainings teams, quality assurance, audits and inspections etc.
6. Act as a consultant or SPOC for various case related activities and maintain knowledge repository of the process updates/ regulatory changes changes on real time.
7. 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.
8. Ensure that quality data is analyzed for any trending and to prepare team for process stabilization.
9. Ensure regulatory compliance by following internal reporting key performance indicators for the unit are met.
10. Independent operations and self-promoted initiatives are expected to interpret and make valuable decisions in ever changing and dynamic requirements from regulators.
11. Being part of transitions to the team and to other teams and certification of the teams on the same.
12. Conduct various interactive activities like workshops, trainings, sessions to educate the team on the existing and on predicted error trends for process improvements.
13. Provide the analytical support for the peers and managers in investigations and analysis of various trends as a part of audits, and inspections.
14. Mentoring the new hires with case processing knowledge transfer, evaluating their progress close to perfection during their initial phases of learning curves.
15. Perform other tasks assigned by the direct manager.

Qualifications:

• Any life sciences/pharmaceutical/healthcare professional graduate (B. Pharmacy, M. Pharmacy, Pharm D, BDS).
• 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

Equal Employment Opportunity Commitment: Teva Pharmaceuticals is committed to providing equal employment opportunities without regard to age, race, religion, sex, disability, sexual orientation, gender identity, veteran status, or any other legally recognized status. Accommodations for the recruitment process are available upon request.

How to Apply: If you meet the qualifications and are excited about this opportunity, please apply online

Tagged as: Good Clinical Practice (GCP)