Hiring Manager-Regulatory Affairs at Teva- Apply before 20th July 2025

Position: Manager – Regulatory Affairs

Job ID: 62544
Location: Bangalore, India
Department: Regulatory Affairs
Industry: Pharmaceuticals / Healthcare / Clinical Research
Last Date to Apply: 20th July 2025

About Teva

Teva Pharmaceuticals is a global pharmaceutical leader and the world’s largest producer of generic medicines. We are committed to increasing access to high-quality healthcare while delivering innovative solutions that improve lives worldwide. Join us in our mission to make a lasting impact on global health.

Job Overview

We are looking for an experienced and detail-oriented Manager – Regulatory Affairs to oversee and manage global regulatory submissions, lifecycle management, and communication with Health Authorities across various markets including US, EU, and APAC. The role involves strategic planning, regulatory document preparation, and cross-functional collaboration to ensure compliance and timely submissions.

Key Responsibilities

• Lead planning and execution of Regulatory Submission Tracker for life cycle management across global markets.

• Develop submission strategies based on regulatory requirements in coordination with cross-functional teams.

• Oversee preparation and submission of variations, renewals, PSURs, DSURs, RMPs, and responses to Health Authority queries.

• Act as regulatory liaison with internal teams and external authorities to ensure timely approvals.

• Maintain regulatory systems, trackers, and databases for accurate, real-time information.

• Contribute to submission and approval KPI metrics.

• Support additional regulatory projects and initiatives as assigned.

Candidate Profile

• Educational Qualification:

  • PharmD / MS in a scientific discipline

  • Master’s in Regulatory Affairs / Quality Assurance is a plus

• Experience:

  • Minimum 8 years in the pharmaceutical industry

  • At least 5 years in Regulatory Affairs with exposure to EU/US/Global markets

  • Experience with lifecycle management and mature product portfolios preferred

• Core Competencies:

  • Strong knowledge of ICH and global regulatory guidelines

  • Excellent verbal and written communication skills

  • Strong analytical, logical thinking, and problem-solving abilities

  • Ability to manage multiple projects, prioritize tasks, and meet tight deadlines

  • Experience working in a cross-functional, global team environment

Why Teva?

• Work with a global leader in the pharmaceutical industry

• Opportunity to engage in meaningful projects that improve patient lives

• Collaborative, diverse, and innovation-driven work culture

• Competitive compensation and professional development

Ready to make a global impact?
Apply now before 20th July 2025 and become a part of Teva’s purpose-driven team.