Lead GPV Professional, ICSR Quality & Metrics

Date: Sep 3, 2025

Location:

Bucharest, Romania, 011171

Company: Teva Pharmaceuticals

Job Id: 63661

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

As Lead GPV Professional, you will support Pharmacovigilance Data Quality and Case Processing Metrics, ensuring accuracy, compliance, and inspection readiness across global PV operations. Reporting to the ICSR Quality & Metrics Team Lead, you will drive oversight, analysis, and continuous improvement of ICSR processes while collaborating cross-functionally to enhance data integrity and operational excellence.

How you’ll spend your day

Ensure compliance with global PV regulations and internal policies, owning key SOPs, WIs, and JAs.
Strengthen ICSR Quality & Metrics by maintaining data integrity, inspection readiness, and seamless submissions.
Transform data into insights by analyzing reports (e.g., QlikSense, V-Safe) and driving meaningful improvements.
Collaborate with cross-functional teams to enhance compliance reporting and streamline processes.
Lead projects that improve case quality, compliance, and performance.
Act as a business owner for selected GPV tools, shaping the SDI strategy.
Promote continuous improvement through root-cause analysis and innovative solutions.
Share knowledge, mentor others, and help the team reach its annual goals and KPIs.

Be part of a team that turns data into action and ensures quality at every step!

Your experience and qualifications

Minimum Master's degree in Life Sciences or another related field.
Minimum of 3 years of Biopharmaceutical/CRO industry experience, including a large international organization.
At least 1 year of direct people/project leadership experience.
Experience in handling Health Authority Inspections.
Project Management experience is an advantage.
Fluent in English.

Reports To

ICSR Quality & Metrics Team Lead

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.