Manager – Regulatory Affairs (Entry-Level / Fresher Friendly)
Location: Bangalore, India – 560064
Category: Regulatory Affairs / Pharmaceutical Operations
Job Type: Full-Time
Experience Required: Fresher / 0–2 Years
Job ID: 65022
Company Overview
Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to making healthcare more affordable and accessible worldwide. Operating across nearly 60 countries, Teva delivers life-changing medicines to over 200 million patients daily and is recognized for many products on the World Health Organization’s Essential Medicines List.
Joining Teva means contributing to innovative healthcare solutions while being part of a diverse, collaborative, and global workforce.
Position Overview
Teva Pharmaceuticals is seeking a Manager – Regulatory Affairs to support International Markets Regulatory Affairs (RA). This is an excellent opportunity for freshers and early-career professionals to gain hands-on experience in regulatory operations, international market submissions, and regulatory documentation.
The role involves coordination of assigned regulatory activities, supporting cross-functional teams, and ensuring compliance with global regulatory requirements.
Key Responsibilities
Support international regulatory affairs operations by completing designated projects and tasks according to Teva’s internal Work Instructions.
Coordinate, prioritize, and monitor tasks related to assigned regulatory activities.
Develop regulatory expertise while solving straightforward problems under moderate guidance.
Maintain regulatory documentation and IT systems in line with internal procedures.
Communicate effectively with Teva units across Europe and International Markets, third-party partners, and relevant health authorities.
Guide and assist junior team members in regulatory processes.
Attend team meetings and provide regular updates to the manager on assigned tasks.
Stay informed about current and upcoming regulatory legislation and guidelines.
Complete assigned trainings through Teva’s internal learning management system.
Qualifications
Educational Requirements:
Master’s in Pharmacy (M.Pharm) or Master’s in Science/Life Sciences.
Alternatively, a Bachelor’s degree with relevant exposure to regulatory principles.
Experience:
Fresher / 0–2 years of experience in pharmaceutical operations, regulatory affairs, or related fields.
Exposure to regulatory documentation within Europe or international markets is a plus.
Skills & Competencies:
Understanding of regulatory submissions, documentation, and international regulatory requirements.
Strong organizational, coordination, and communication skills.
Ability to work collaboratively in a cross-functional, global team.
Detail-oriented with proficiency in regulatory IT systems.
Reporting
Reports To: Senior Regulatory Affairs Staff / Manager
Equal Employment Opportunity
Teva Pharmaceuticals is committed to equal opportunity employment and fostering a diverse and inclusive workplace. Employment decisions are made without regard to age, race, color, religion, gender, disability, sexual orientation, gender identity, veteran status, or any other legally protected status. Reasonable accommodations are available for candidates requiring support during the recruitment process.
Why Join Teva?
Gain exposure to international regulatory affairs operations and documentation.
Launch your career in a globally recognized pharmaceutical company.
Work in a collaborative, diverse, and supportive environment.
Build expertise in regulatory compliance, submission strategies, and cross-border regulatory processes.
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