Regulatory Affairs Associate I Job at Teva Pharmaceuticals in Navi Mumbai. Apply for global regulatory publishing role with strong growth and exposure opportunities.
The pharmaceutical regulatory domain continues to grow rapidly as global companies expand their compliance and submission operations. Teva Pharmaceuticals is currently hiring talented professionals for the role of Regulatory Affairs Associate I in Navi Mumbai. This opportunity is ideal for candidates who have foundational regulatory publishing experience and are looking to build a long-term career in global submissions and compliance.
If you have 1–3 years of experience in regulatory publishing and want to work with international markets like the US and EU, this role can provide excellent exposure and growth potential. Regulatory Affairs Associate I Job at Teva Pharmaceuticals in Navi Mumbai
Company Overview
Teva Pharmaceuticals is a globally recognized biopharmaceutical company known for its strong presence in both generics and innovative medicines. The company operates across multiple therapeutic areas and is committed to improving healthcare access worldwide. With operations in several countries and a diverse workforce, Teva offers a collaborative and inclusive work environment where employees can contribute to meaningful healthcare advancements.
Teva is also known for providing structured career development programs and access to modern regulatory technologies that help professionals grow in highly specialized domains. Regulatory Affairs Associate I Job at Teva Pharmaceuticals in Navi Mumbai
Job Location & Employment Type
- Location: Navi Mumbai, Maharashtra, India
- Job Type: Full-Time
- Department: Regulatory Affairs – Submission Publishing
- Job ID: 66406
Open Position Details
Teva is recruiting for the position of Regulatory Affairs Associate I, primarily focused on regulatory publishing activities. The role involves supporting submission preparation and ensuring that regulatory documents meet international standards and timelines.
This position will involve working closely with regulatory teams and supporting submission activities across major global markets. Regulatory Affairs Associate I Job at Teva Pharmaceuticals in Navi Mumbai
Key Roles & Responsibilities
Candidates selected for this role will be responsible for handling various regulatory publishing and submission-related activities, including:
- Preparing and publishing electronic regulatory submissions in formats such as eCTD and NeeS
- Managing lifecycle and post-approval submissions for international regulatory agencies
- Ensuring timely dispatch of regulatory submissions while maintaining accuracy and compliance
- Performing document-level formatting and validation for submission readiness
- Conducting quality checks to ensure adherence to regulatory guidelines
- Collaborating with cross-functional scientific and regulatory teams
- Troubleshooting technical publishing issues and ensuring smooth submission workflows
- Maintaining knowledge of global regulatory publishing standards
- Using regulatory tools and platforms for submission management
- Ensuring all submission documents align with regulatory authority requirements
This role requires strong attention to detail, technical proficiency, and the ability to work within strict submission timelines. Regulatory Affairs Associate I Job at Teva Pharmaceuticals in Navi Mumbai
Eligibility Criteria
Educational Qualification
Candidates must have one of the following academic backgrounds:
- B.Pharm
- M.Pharm
- Master’s Degree in Life Sciences
A strong academic background in pharmaceutical sciences or related fields is preferred. Regulatory Affairs Associate I Job at Teva Pharmaceuticals in Navi Mumbai
Experience Required
- 1 to 3 years of relevant industry experience
- Prior exposure to regulatory publishing is preferred
- Experience working with EU or US submissions will be an added advantage
Freshers are not typically considered for this role unless they have strong internships in regulatory publishing.
Skills Required
To succeed in this position, candidates should possess the following skills:
- Understanding of regulatory submission formats like eCTD and NeeS
- Familiarity with ICH guidelines and submission standards
- Good written and verbal English communication skills
- Ability to work in a globally diverse team environment
- Strong documentation and quality-checking abilities
- Basic understanding of regulatory IT systems
Knowledge of the following tools will be beneficial:
- Veeva Vault
- Lorenz Validator
- Adobe Acrobat
- Global Insight
- ISI Toolbox
Candidates who are comfortable using regulatory software tools will have a competitive advantage.
Salary & Benefits
Salary and compensation will be as per company norms and aligned with experience and qualifications.
Employees working at Teva may also receive additional benefits such as:
- Paid annual leave
- Career development opportunities
- Internal learning platforms
- Flexible work policies (role dependent)
- Health and wellness support
- Global exposure and internal mobility options
Selection Process
The selection process may include the following stages:
- Initial application screening
- HR discussion
- Technical interview with regulatory team
- Final selection and offer rollout
Shortlisted candidates will be contacted directly by the company for further steps. Regulatory Affairs Associate I Job at Teva Pharmaceuticals in Navi Mumbai
How to Apply
Interested candidates should apply through the company’s official career portal or the original job listing page.
Ensure your resume highlights:
- Regulatory publishing experience
- Submission formats handled
- Software tools used
- Global submission exposure
Applications submitted with detailed regulatory experience have higher chances of shortlisting. Regulatory Affairs Associate I Job at Teva Pharmaceuticals in Navi Mumbai
Important Dates
- Candidates are encouraged to apply at the earliest as positions may close once filled.
Why Apply for This Pharma Job?
Working with Teva Pharmaceuticals offers several career advantages, especially for professionals aiming to grow in regulatory affairs. Here’s why this opportunity stands out:
- Exposure to international regulatory submissions
- Opportunity to work with global healthcare teams
- Access to advanced regulatory technologies
- Structured career development pathways
- Stable work environment in a leading pharma company
- Learning opportunities in global compliance frameworks
For professionals looking to transition into advanced regulatory roles, this position can act as a strong stepping stone. Regulatory Affairs Associate I Job at Teva Pharmaceuticals in Navi Mumbai
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform created to help job seekers find pharmaceutical career opportunities. We are not directly associated with Teva Pharmaceuticals or any other company. Candidates are advised to verify all details from official company sources before applying. We do not charge any fee for job information. Regulatory Affairs Associate I Job at Teva Pharmaceuticals in Navi Mumbai
Final Call-to-Action
If you have experience in regulatory publishing and want to work with a globally respected pharmaceutical organization, this opportunity at Teva Pharmaceuticals should not be missed. Update your resume and apply as soon as possible to increase your chances of selection. Stay connected with IndiaPharmaJobs.in for the latest verified pharma jobs across India and global markets. Regulatory Affairs Associate I Job at Teva Pharmaceuticals in Navi Mumbai
