Teva Regulatory Affairs Associate job 2026 in Navi Mumbai. Apply for RA publishing role with global exposure and career growth opportunities.
Company Overview
Teva Pharmaceuticals is one of the world’s leading biopharmaceutical companies, known for its strong presence in both innovative medicines and high-quality generic products. With operations spanning multiple countries, Teva focuses on improving patient access to essential medicines across therapeutic areas such as neuroscience, immunology, and chronic diseases.
The company is recognized for its collaborative work culture, innovation-driven approach, and commitment to employee development. Teva provides professionals with opportunities to grow in a global regulatory and pharmaceutical environment while contributing to healthcare advancements.
Job Overview (Job Details)
| Particulars | Details |
|---|---|
| Company Name | Teva Pharmaceuticals |
| Job Title | Regulatory Affairs Associate I (RA Publishing) |
| Job Location | Navi Mumbai, India |
| Job Type | Full-Time |
| Department | Regulatory Affairs |
| Qualification | B.Pharm / M.Pharm / Life Sciences |
| Experience | 1–3 Years |
| Application Mode | Online |
| Job ID | 66406 |
Job Location & Employment Type
This position is located in Navi Mumbai, Maharashtra, and is a full-time opportunity within the Regulatory Affairs department. The role focuses on regulatory publishing activities for global markets including the US, EU, and Canada.
Open Positions / Department Details
- Role: Regulatory Affairs Associate I – RA Publishing
- Department: Regulatory Submission Management
- Reporting To: Manager – Regulatory Submission Management
The role involves handling regulatory submission publishing processes and ensuring compliance with global regulatory standards.
Key Roles & Responsibilities
The selected candidate will play a key role in managing and publishing regulatory submissions. Responsibilities include:
- Publishing and dispatching eCTD submissions for major global markets such as the US, EU, and Canada
- Handling lifecycle and post-approval submissions with accuracy and timeliness
- Performing document-level publishing tasks and resolving technical issues
- Conducting quality control checks to ensure submission readiness as per regulatory guidelines
- Collaborating with scientific and regulatory teams for submission planning and execution
- Maintaining up-to-date knowledge of publishing standards and regulatory requirements
- Working with regulatory IT tools and systems to support submission processes
- Ensuring compliance with ICH guidelines and electronic submission standards
Eligibility Criteria
Education
- B.Pharm or M.Pharm
- Master’s degree in Life Sciences
Experience
- 1 to 3 years of experience in regulatory affairs or publishing
- Experience in EU and US regulatory publishing is preferred
Skills Required
- Knowledge of ICH guidelines and eCTD/NeeS submission formats
- Familiarity with regulatory publishing tools such as Global Insight, Veeva Vault, ISI Toolbox, Adobe Acrobat, and Lorenz Validator
- Understanding of regulatory IT systems and document management processes
- Strong written and verbal communication skills in English
- Ability to work in a global and culturally diverse environment
- Attention to detail and ability to meet strict timelines
Salary & Benefits
- Salary: As per company norms
- Flexible working options (role-dependent)
- Paid leaves and employee wellness programs
- Career development through internal learning platforms
- Opportunities for global exposure and internal mobility
- Supportive and inclusive workplace culture
Selection Process
The recruitment process may include:
- Online application submission
- Resume shortlisting
- Technical interview (regulatory affairs and publishing knowledge)
- HR discussion
- Final selection
How to Apply
Interested candidates can apply online through the official careers portal of Teva Pharmaceuticals.
- Job ID: 66406
- Location: Navi Mumbai, India
Candidates are advised to apply as soon as possible to avoid missing this opportunity.
Important Dates
- Last Date to Apply: Not specified
Why Apply for This Pharma Job?
This role offers an excellent opportunity to build a career in regulatory affairs within a globally recognized pharmaceutical company. Candidates will gain hands-on experience in regulatory publishing for international markets, which is a highly valuable skill in the pharma industry.
Working at Teva allows professionals to engage with global regulatory frameworks, advanced submission technologies, and cross-functional teams. It is an ideal role for candidates aiming to specialize in regulatory affairs and submission management.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with Teva Pharmaceuticals or any recruiter. We do not charge any fees for job applications. Candidates should verify all information from official sources before applying.
Final Call-to-Action
Candidates with regulatory affairs experience looking to advance their careers in a global pharmaceutical environment should apply at the earliest opportunity.
