Regulatory Affairs Associate I – Teva Pharmaceuticals | Pharma Graduates
- Teva Hiring Regulatory Affairs Associate I in Navi Mumbai | 1–3 Years Pharma Regulatory Role
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Background:
- Experience Required:
- Skills Required:
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- 1. Is this role suitable for freshers?
- 2. What is eCTD in regulatory affairs?
- 3. What tools are required for this role?
- 4. What career growth can I expect?
- Summary
Teva Hiring Regulatory Affairs Associate I in Navi Mumbai | 1–3 Years Pharma Regulatory Role
Looking to build a career in regulatory affairs and global submissions? Teva Pharmaceuticals is hiring a Regulatory Affairs Associate I for its regulatory publishing team in Navi Mumbai. This role is ideal for candidates with 1–3 years of experience in regulatory publishing, especially those with exposure to EU, US, and Canada submissions.
This full-time position offers hands-on experience in eCTD publishing, lifecycle management submissions, and global regulatory compliance, making it a strong opportunity for professionals aiming to grow in high-demand regulatory affairs careers.
Company Overview
Teva Pharmaceuticals is one of the world’s leading biopharmaceutical companies, combining a strong generics portfolio with innovative specialty medicines. With operations across global markets, Teva focuses on improving patient access to high-quality treatments in areas such as neuroscience and immunology.
The company is known for its robust regulatory systems, global presence, and commitment to compliance, making it a preferred organization for professionals in regulatory affairs and pharmaceutical operations.
Job Role & Responsibilities
As a Regulatory Affairs Associate I, you will be responsible for regulatory publishing activities and ensuring timely, high-quality submissions to global health authorities.
Key Responsibilities:
- Publish and dispatch complex eCTD submissions for EU, US, and Canada markets
- Handle post-approval and lifecycle management submissions
- Perform document-level publishing and resolve technical document issues
- Conduct quality control checks to ensure submission readiness
- Collaborate with scientific and regulatory teams for planning and submission activities
- Maintain knowledge of publishing standards and regulatory guidelines
- Work with tools such as Veeva Vault, Global Insight, ISI Toolbox, and Lorenz Validator
- Ensure compliance with ICH, eCTD, NeeS, and agency-specific requirements
Eligibility / Qualifications
Educational Background:
B.Pharmacy, M.Pharmacy, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Life Sciences
Experience Required:
- 1–3 years of experience in regulatory publishing or regulatory affairs
- Experience in EU and US regulatory submissions preferred
- Understanding of eCTD and regulatory submission formats
Skills Required:
- Strong knowledge of regulatory IT systems and publishing tools
- Good understanding of ICH guidelines and submission standards
- Excellent written and verbal communication skills
- Attention to detail and ability to manage timelines
- Ability to work in global and cross-cultural environments
Location & Salary
- Location: Navi Mumbai, India
- Job Type: Full-time
- Salary: Competitive salary package with performance-based benefits
Teva offers strong employee benefits including flexible work options, career development programs, health support, and global growth opportunities within the pharmaceutical industry.
Application Process
Interested candidates can apply through the official Teva careers portal:
Apply Here: https://careers.teva/job/Navi-Mumbai-Regulatory-Affairs-Associate-I-Indi-400706/1377703600/
Frequently Asked Questions (FAQs)
1. Is this role suitable for freshers?
No, this position requires 1–3 years of experience in regulatory affairs or publishing.
2. What is eCTD in regulatory affairs?
eCTD (electronic Common Technical Document) is a standard format used for submitting regulatory information to health authorities.
3. What tools are required for this role?
Candidates should be familiar with Veeva Vault, Lorenz Validator, ISI Toolbox, and similar publishing systems.
4. What career growth can I expect?
You can grow into roles such as Regulatory Affairs Specialist, Publishing Lead, or Global Regulatory Manager.
Summary
| Category | Details |
|---|---|
| Company | Teva Pharmaceuticals |
| Vacancies | Regulatory Affairs Associate I |
| Required Education | B.Pharmacy, M.Pharmacy, MSc, Life Sciences |
| Experience | 1–3 years |
To apply for this job please visit careers.teva.
