Teva Pharmaceuticals Hiring Regulatory Affairs Associate I in Navi Mumbai. Explore responsibilities, qualifications, skills required, and step-by-step application process.
Teva Pharmaceuticals, a global leader in the generic pharmaceutical industry, has announced an opportunity for the role of Regulatory Affairs Associate I at its Navi Mumbai location. This position offers a promising career track for individuals who want to build their expertise in the regulatory domain, specifically focusing on regulatory submissions, eCTD publishing, and lifecycle management processes. Candidates with strong knowledge of regulatory documentation, IT systems, and global submission standards can find this role both challenging and rewarding. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
This long-format post explains the job responsibilities, required qualifications, desired skills, and complete details about the hiring process. Whether you are a fresh professional with minimal experience or someone with up to three years in regulatory publishing, this role at Teva Pharmaceuticals may be a significant milestone in your career. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Key Highlights
| Particular | Details |
|---|---|
| Company Name | Teva Pharmaceuticals |
| Job Role | Regulatory Affairs Associate I |
| Job Location | Navi Mumbai, Maharashtra |
| Experience Required | 1–3 years (Regulatory Publishing experience preferred) |
| Education Qualification | B.Pharm, M.Pharm, or Master’s in Life Sciences |
| Department | Regulatory Submission Management |
| Job ID | 64525 |
| Application Mode | Online |
About Teva Pharmaceuticals
Teva Pharmaceuticals is recognized as one of the largest manufacturers of generic medicines across the globe. With operations in nearly 60 countries and a workforce representing diverse nationalities, Teva has built a strong legacy in making healthcare more accessible and affordable. The company’s products reach over 200 million people daily, reflecting Teva’s scale and commitment to global health. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Teva’s mission revolves around improving the well-being of patients worldwide by producing high-quality medicines and driving innovation in pharmaceuticals. Working at Teva means being part of a global ecosystem where scientific expertise, regulatory excellence, technological advancement, and quality manufacturing come together to create meaningful impact. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Job Opportunity: Regulatory Affairs Associate I
The role of Regulatory Affairs Associate I – RA Publishing primarily focuses on handling regulatory submissions using established global publishing standards. The candidate will work closely with internal regulatory teams and scientific personnel to ensure the accuracy, completeness, and timely submission of documents to agencies across multiple regions such as the United States, Canada, and the European Union.
This position requires high attention to detail, strong technical skills, and the ability to coordinate with global teams. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Detailed Roles and Responsibilities
The responsibilities associated with the Regulatory Affairs Associate I position revolve around document publishing, regulatory submissions, and maintaining compliance with global regulatory guidelines. Below is an expanded breakdown of the daily tasks and expectations for this role. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
1. Managing eCTD Submissions
The candidate will be responsible for preparing, compiling, and publishing eCTD submissions. These include major regulatory submissions as well as routine lifecycle management activities for the EU, US, and Canada markets. Ensuring accuracy and consistency in all eCTD modules is an essential part of the job.
2. Post-Approval Submissions
Regulatory professionals often handle post-approval changes, and this role requires the candidate to prepare and publish high-quality submissions related to updates, variations, and amendments after the initial approval of a product.
3. Document-Level Publishing and Troubleshooting
The candidate will review, format, and troubleshoot regulatory documents before they are published. This includes checking file formats, correcting technical errors, ensuring proper bookmarks and hyperlinks, and validating that all files meet agency requirements.
4. Quality Control of Submission Documents
Every regulatory submission must undergo strict quality checks. The candidate must perform document-level QC to ensure that content, formatting, and structure meet the guidelines outlined by ICH, regional agencies, and internal standards.
5. Collaboration with Scientific and Regulatory Teams
A large part of the role includes working alongside scientific personnel and regulatory associates to ensure timely planning and execution of submissions. The position requires excellent communication and coordination skills.
6. Maintaining Knowledge of Global Standards
Regulatory guidelines, including ICH and eCTD specifications, undergo periodic updates. The candidate must stay informed about the latest regulatory publishing standards, internal SOPs, and new global submission requirements.
7. Using Regulatory IT Tools and Systems
The role requires basic to intermediate proficiency with tools such as: Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
- Global Insight
- Veeva Vault
- ISI Toolbox
- Lorenz Validator
- Adobe Acrobat
These tools are essential for preparing, validating, and publishing electronic submissions. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Required Skills and Experience
Education
Candidates must possess one of the following qualifications:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- Master’s degree in Life Sciences
Experience
- Minimum 1 year and up to 3 years of experience
- Hands-on experience in regulatory publishing for EU and US markets is preferred
Technical Skills
- Knowledge of ICH guidelines
- Understanding of eCTD, NeeS, and paper formats
- Ability to work with regulatory publishing tools
- Document formatting and QC skills
Soft Skills
- Strong written and spoken English
- Ability to understand and respect cultural diversity
- Sharp attention to detail
- Good communication and collaboration skills
Why Consider a Career at Teva Pharmaceuticals?
Working at Teva Pharmaceuticals provides exposure to global regulatory standards and high-impact pharmaceutical submissions. The company is known for offering:
- Growth opportunities in regulatory affairs
- Global project exposure
- Structured career development programs
- A diverse and inclusive workplace
- Opportunities to work with advanced regulatory systems and technology
For professionals aiming to specialize in regulatory submissions and publishing, this role offers a unique platform to grow and make meaningful contributions. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Department and Reporting Structure
This position falls under the Regulatory Submission Management department.
The selected candidate will report directly to the Manager – Regulatory Submission Management. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Commitment to Equal Employment Opportunity
Teva Pharmaceuticals follows a strict equal employment opportunity policy. The company does not discriminate on the basis of age, gender, religion, color, disability, sexual orientation, pregnancy, veteran status, ethnic origin, or any other legally protected category. Teva ensures a respectful, inclusive, and supportive environment for all applicants and employees. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
How to Apply for Teva Pharmaceuticals Regulatory Affairs Associate I Position
Candidates interested in applying can follow the steps below: Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
- Visit Teva Pharmaceuticals’ official careers page.
- Use the job search option and enter Job ID: 64525 or search for Regulatory Affairs Associate I – Navi Mumbai.
- Read the full job description and eligibility criteria.
- Register or log in with your email ID.
- Fill out the online application form with accurate personal and academic details.
- Upload your updated resume and any relevant documents.
- Submit the application and wait for a confirmation email.
Shortlisted candidates will be contacted by the recruitment team for further rounds, which may include technical assessments, interviews, and HR discussions. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
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