Lead GPV Professional, ICSR Conventions

Teva; Navi Mumbai; On-site; INR 3,500,000 - 6,000,000; Full time

Job summary

Teva India is seeking a Lead GPV Professional to drive regulatory compliance for System Data Innovation (SDI) within a large, global biopharma setup. You will contribute to GPV ICSR Conventions and lead cross‑functional projects ensuring audit readiness and robust change control processes.

The role requires 7+ years in biopharma/CRO, expertise in inspections, project leadership, and strong AI/technical skills.

Qualifications

• Minimum 7 years of Biopharmaceutical/CRO industry experience.
• Experience in Health Authority inspections/third-party audits.
• Project management experience required.
• AI/Technical expertise is a must.
• Knowledge of Veeva Vault Safety is desired.
• Fluent in English.

Responsibilities

• Ensure regulatory compliance and inspection readiness for System Data Innovation (SDI).
• Apply global PV vision and GPV ICSR Conventions strategy in projects.
• Drive continuous improvement activities including V-safe enhancements.
• Coordinate inspection/audit readiness and attend interviews on Veeva Vault Safety.
• Produce SDI SOPs/WIs and manage change controls; coordinate gaps and CAPA writing.

Skills

Biopharma/CRO exp

Inspections/audits

Project management

AI/Technical exp

Veeva Vault Safety

English fluency

Job description

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

• The Lead GPV Professional, part of GPV ICSR Conventions acts as active contributor to all SDI processes and compliance topics, such as: SDI Audits & Inspections management, Training of SDI section members and LSOs/PV functions on SDI process related changes, gap assessments, knowledge management, SDI change control management, coordination of SDI related risk cards and remediation plans, coordination of SDI related deviations and CAPAs.
• The Lead GPV Professional, part of the GPV ICSR Conventions has an active contribution to the one-company operational business-related continuous improvement projects such as GPV; TGO (Quality) in relation to GPV/patient safety aspects and other special projects, end-to-end, for all Teva products worldwide.

How You’ll Spend Your Day

• Contributes directly and continuously towards ensuring the company’s compliance with laws and regulations to fulfil regulatory compliance and inspection readiness concerning all aspects of System Data Innovation(SDI).
• Acts as individual contributor, by applying the global PV vision and strategy for GPV ICSR Conventions and its regulatory compliance in all sub-areas of responsibility and corresponding projects. Drives the change in line with the vision and strategy, by assuming responsibility of various projects, in accordance with the group’s needs and plans.
• Takes part to continuous improvement activities, including efficiency, quality and compliance, including but not limited to the V-safe functionalities analysis and enhancements design.
• Part of a team with direct and shared responsibilities around the following: Inspection/audit readiness coordination and interview attendance on Veeva Vault Safety related aspects. Content provider for SDI, GPV ICSR Conventions related written procedures/ Standard Operating Procedures (SOPs) and Working Instructions (WIs); Change control management for handling of process changes; Gap assessments; SDI training responsibilities for SDI functions +LSOs/regions; Knowledge management coordination; GPV ICSR Conventions deviation and CAPA writing coordination.
• Takes part to the boarding and training processes of new SDI colleagues;
• Contributes to the establishment of new and strengthened synergies with interfacing functions as well as intra-functionally within SDI with the following sub streams:ICSR Global OperationS; ICSR Quality&Metrics; Project Management and Innovation; Systems and Data Solutions driving the strategy and proactively championing for inter- and intra- face engagement and optimal ways of working.

Your Skills and Experience

• Minimum of 7 years of Biopharmaceutical/CRO industry experience, including a large international organization.
• Experience in handling Health Authority Inspections/third party audits.
• Project Management experience is needed.
• AI / Technical expertise is a must.
• Knowledge is using Veeva Vault Safety is desired.
• Fluent in English.

How We’ll Take Care of You

At Teva India, care is at the heart of how we work. From your first day, you’ll be welcomed into a people-first culture built on inclusion, respect, and belonging.

That support extends to you and your loved ones through benefits designed for real life. These include comprehensive medical insurance, OPD coverage, annual health checkups, term life and accident insurance, and confidential emotional wellbeing support through our Optum Employee Assistance Program. You’ll also enjoy healthy meals at work, holistic wellbeing initiatives, and volunteering programs that help you give back to the community.

• comprehensive medical insurance
• OPD coverage
• annual health checkups
• term life and accident insurance
• confidential emotional wellbeing support through our Optum Employee Assistance Program

Your growth matters too. You’ll have opportunities to build future-ready skills, collaborate on projects with global teams, explore internal career opportunities, and learn through programs such as our AI-enabled Teva Twist program, R&D Academy, continuing education, and mentorship.

Join our vibrant workplace, where we celebrate milestones, festivals, achievements, and community impact together.

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.