Regulatory Affairs Associate I – Teva Pharmaceuticals | Pharma Graduates
- Regulatory Affairs Associate I – Join Teva’s Global Labeling Team
- Job Location
- About Teva Pharmaceuticals
- Key Responsibilities
- Editorial & Labeling Tasks
- Translation Management
- Process and Compliance Monitoring
- Administrative Support
- The opportunity
- How you’ll spend your day
- Your experience and qualifications
- Knowledge and Skills
- Apply Online
- Summary Table
Regulatory Affairs Associate I – Teva Pharmaceuticals | Pharma Graduates | Bangalore Location | 1+ Year Experience
Apply for Regulatory Affairs Associate I at Teva Pharmaceuticals in Bangalore. Open to Pharma graduates with 1+ year of regulatory affairs or editorial experience.
Regulatory Affairs Associate I – Join Teva’s Global Labeling Team
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📱 Join Click HereTeva Pharmaceuticals, a global leader in generic and specialty medicines, is hiring a Regulatory Affairs Associate I for its Bangalore location. This opportunity is ideal for pharmaceutical and medical science graduates with basic knowledge or hands-on experience in regulatory affairs, European pharmaceutical law, or editorial roles.
As a Regulatory Affairs Associate, you will support the Labeling and Translation Management teams for EU Centralized Procedures (CPs), ensuring pharmaceutical and medically accurate product labeling across markets.
Job Location
Location: Bangalore, India
Position Type: Full-Time, Associate Level
About Teva Pharmaceuticals
Teva operates in over 60 countries and delivers high-quality generic and specialty medications to more than 200 million people every day. Our employees are united by a shared mission: to make good health more affordable and accessible. At Teva, your work contributes to a healthier world.
Key Responsibilities
Editorial & Labeling Tasks
- Review and edit product labeling materials (SmPC, PIL, packaging) based on templates
- Adapt texts using QRD templates and perform proofreading
- Maintain product information in internal systems (e.g., GRIDS)
- Act as super-editor in GRIDS for consistency and regulatory compliance
Translation Management
- Coordinate all translation steps post-translation request for EU CPs
- Liaise with internal stakeholders, local markets, and translation agencies
- Manage translation reviews, QC checks, and final document submissions
Process and Compliance Monitoring
- Track EU regulatory environment updates, guidelines, and innovations
- Support cross-departmental inquiries and collaborate with service providers
Administrative Support
- Manage service contracts, purchase requests, and invoice releases in SAP/ARIBA
The opportunity
- To organize and perform required regulatory tasks to maintain existing EU procedures in line with current regulations, guidelines and in-house standards
- To obtain regulatory approvals for defined European procedures, ensuring high quality data and standards are used in all regulatory applications
- To ensure high quality documents and standards are used in preparation of all regulatory applications to achieve rapid and successful assessment.
- To give regulatory support to project teams, stakeholders and other sites, as require
How you’ll spend your day
- Prepare, compile, review and submit high quality submissions for all required post-approval activities in accordance with EU legislation and in-house standards.
- Responsibility for MA compliance with both legislation and business needs.
- Prioritize, plan and monitor submissions for allocated procedures while documenting and informing involved parties of progress.
- Ensure approvals are secured within the stipulated timelines for designated projects.
- Maintain registration documentation and associated electronic databases, in line with in-house procedures.
- Provide regulatory support and product information for all internal and external customers, stakeholders and TEVA project teams.
- Communicate with other Teva departments across Europe and European Agencies regarding proposed and pending submissions.
- Maintain and develop awareness of current/pending regulatory legislation and guidelines.
- Fulfilling other allocated department duties and ad-hoc needs at the direction of Senior Regulatory Affairs personnel.
- Awareness of regulatory legislation and guidelines
Your experience and qualifications
- Required Degree: M Pharm or M.Sc.
- Total years of experience required for the role: 2 to 3 years in Post approval Regulatory affairs
- Overall Pharma industry experience: 2 to 3 years
- Desirable to have EU experience and knowledge of European regulatory procedures
Knowledge and Skills
- Desirable to have EU member state experience and knowledge of European regulatory procedures.
- Understanding of processes and departments within a pharmaceutical company.
- Excellent oral and written communication
- Ability to work under pressure and to tight time deadlines
- Effective time and organisation management
- Negotiation
- Initiative
- Analytical (Data and Documentation)
- Computer literacy
- Teamwork and collaboration
- Attention to detail
- Planning and Organisation
Apply Online
If you are passionate about global healthcare compliance and have the necessary background in Pharma or Life Sciences, this could be your next step forward.
📩 Send your resume to: Rekha.Rathod@teva.co.in
🔗 Or apply online: Click to Apply
Summary Table
| Company Name | Current Vacancies in Departments |
|---|---|
| Teva Pharmaceuticals | Regulatory Affairs – Labeling & Translation |
| Required Education | Experience Required |
|---|---|
| D.Pharm / B.Pharm / Life Sciences Diploma or Degree | 1+ year in Regulatory or Editorial roles |
To apply for this job please visit careers.teva.