Teva Pharma Hiring for Regulatory Affairs Associate I in Bangalore with 2–3 years experience. Apply for global regulatory affairs role.
Teva Pharmaceuticals, one of the world’s leading pharmaceutical manufacturers, has announced an opening for the position of Regulatory Affairs Associate I at its Bangalore location. This long-format article provides a complete overview of the job role, responsibilities, qualifications, required experience, benefits, and how to apply. The content is optimized for SEO and ideal for job-related websites, pharma job portals, and regulatory affairs career platforms. Teva Pharma Hiring for Regulatory Affairs Associate I
About Teva Pharmaceuticals
Teva Pharmaceuticals is recognized globally as the largest manufacturer of generic medicines and a trusted provider of high-quality pharmaceutical solutions. The organization operates in nearly 60 countries and serves over 200 million patients worldwide every single day through its broad portfolio of generic, specialty, and over-the-counter medicines. Teva Pharma Hiring for Regulatory Affairs Associate I
The company is widely known for its commitment to affordability, accessibility, and healthcare innovation. Many Teva-manufactured products feature on the World Health Organization’s Essential Medicines List, highlighting its strong contribution to public health globally.
With a diverse workforce and a culture that encourages collaboration, growth, and global impact, Teva offers an excellent environment for pharmaceutical professionals seeking to advance their careers in regulatory affairs. The Bangalore site is a major hub supporting global regulatory operations, including Europe and various international markets. Teva Pharma Hiring for Regulatory Affairs Associate I
Position Overview: Regulatory Affairs Associate I
Job Title: Regulatory Affairs Associate I
Date Posted: November 14, 2025
Job ID: 64000
Location: Bangalore, Karnataka, 560064
Company: Teva Pharmaceuticals
The Regulatory Affairs Associate I will support Teva’s International Markets Regulatory Affairs (RA) team. This role focuses on executing regulatory tasks aligned with internal procedures and international regulatory frameworks. It requires individuals who can manage documentation, ensure compliance, work with global teams, and contribute effectively to submission-related workflows. Teva Pharma Hiring for Regulatory Affairs Associate I
This position is suitable for professionals with 2–3 years of experience in Regulatory Affairs, R&D, Development, or QA—particularly those aiming to build a long-term career in global regulatory operations. Teva Pharma Hiring for Regulatory Affairs Associate I
Key Responsibilities
The Regulatory Affairs Associate I role involves day-to-day activities essential to regulatory compliance and submission management for international markets. Responsibilities include: Teva Pharma Hiring for Regulatory Affairs Associate I
1. Completing Assigned Regulatory Projects
The selected candidate will handle specific regulatory projects and tasks related to International Markets RA. These activities must be completed in alignment with internal Work Instructions and under the supervision of senior regulatory team members and the reporting manager.
The work includes preparation, maintenance, and submission of regulatory documents required for varied country regulations across multiple markets.
2. Managing Regulatory Documentation and IT Systems
Accurate documentation is essential in regulatory operations. Responsibilities include:
- Maintaining regulatory documents as per internal documentation standards.
- Updating regulatory IT systems and databases.
- Ensuring all data entries comply with quality standards and regulatory expectations.
- Supporting document lifecycle management through systems like Veeva Vault.
3. Ensuring Timely and Compliant Task Execution
This includes:
- Completing tasks within designated timelines.
- Maintaining trackers with accurate, real-time updates.
- Meeting compliance standards required for global regulatory functioning.
Time management and adherence to internal procedures play a crucial role in achieving team goals.
4. Communication and Coordination with Internal Teams and Health Authorities
A major part of the role includes interacting with:
- Cross-functional Teva teams across International Markets
- External third parties
- Health Authorities (for submissions, clarifications, compliance matters)
Good communication skills are necessary to ensure smooth coordination for regulatory submissions, document requests, and compliance queries. Teva Pharma Hiring for Regulatory Affairs Associate I
5. Supporting Additional Department Tasks
Other responsibilities include:
- Completion of internal training modules through Teva’s learning management system.
- Participating in department meetings and providing timely updates.
- Supporting ad-hoc tasks assigned by senior members.
This ensures continuous learning and involvement in various regulatory processes.
6. Staying Updated with Regulatory Guidelines
The candidate must maintain awareness of:
- Current and evolving international regulatory requirements
- Updated guidelines affecting Teva’s product portfolio
- Country-specific regulatory changes across Europe and international markets
This helps ensure compliance and effective preparation of regulatory submissions.
Required Qualifications
To be eligible for the Regulatory Affairs Associate I role, candidates must fulfill the following qualification criteria: Teva Pharma Hiring for Regulatory Affairs Associate I
Educational Requirements
- Masters in Pharmacy (M.Pharm)
- Masters in Science / Life Sciences
- Or a college/university degree that provides strong theoretical and scientific understanding suitable for regulatory work.
This ensures adequate scientific foundation for reviewing pharmaceutical data and understanding regulatory standards.
Required Experience
Teva requires:
- 2–3 years of experience in the pharmaceutical industry.
- Preferably in Regulatory Affairs, but experience in R&D, Product Development, or Quality Assurance will also be considered.
Additional expectations:
- Experience preparing or managing regulatory documents for Europe and/or International Markets.
- Exposure to dossier compilation, variation submissions, renewals, or market-specific regulatory communication.
Skill Requirements and Knowledge Areas
The ideal candidate must possess the following:
1. Regulatory Knowledge
- Understanding of regulatory concepts, documentation formats, and submission processes.
- Ability to resolve routine regulatory issues using internal procedures.
2. Technical Skills
- Proficiency in regulatory IT systems.
- Good working knowledge of Office 365 applications.
- Experience with Veeva Vault will be advantageous.
3. Compliance Awareness
- Strong focus on regulatory compliance.
- Understanding of global standards and documentation requirements.
4. Organizational & Project Management Skills
- Ability to prioritize tasks and manage multiple assignments.
- Knowledge of basic project management principles.
5. Problem-Solving Abilities
- Identifying challenges that need escalation.
- Using judgment within defined guidelines.
6. Language Advantage
- Knowledge of French or German is considered an added advantage, especially for European submissions.
Teva Pharmaceuticals Equal Employment Opportunity Commitment
Teva is committed to maintaining a diverse, welcoming, and inclusive workplace environment. The company ensures equal employment opportunities without discrimination based on age, gender, race, disability, pregnancy, nationality, orientation, identity, or any legally protected status. Teva Pharma Hiring for Regulatory Affairs Associate I
Applicants requiring accommodation during the recruitment process are encouraged to disclose their needs. All information is treated confidentially to support an accessible interview experience. Teva Pharma Hiring for Regulatory Affairs Associate I
How to Apply for Teva Pharmaceuticals Regulatory Affairs Associate I Position
Interested and eligible candidates can apply online through Teva’s official careers website. Follow the steps below: Teva Pharma Hiring for Regulatory Affairs Associate I
- Visit Teva’s official Careers Page.
- Search for the Job ID: 64000 or role title “Regulatory Affairs Associate I”.
- Open the job listing and click on Apply Now.
- Create or log in to your Teva candidate account.
- Upload your updated resume and complete the online application form.
- Submit the application and monitor your email for further communication from Teva’s HR team.
Make sure your resume highlights your regulatory experience, IT system knowledge, and compliance exposure to increase your selection chances. Teva Pharma Hiring for Regulatory Affairs Associate I
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