Teva Pharmaceuticals Industries Limited is a multinational company headquartered in Jerusalem, operating actively in more than 60 countries worldwide. Teva is also renowned as a leading pharmaceutical company in producing generic medicines to improve lives worldwide. Teva has transformed from a small wholesale drug business into the world’s top pharmaceutical company. For more details about the company, you can visit Committed to Better Health | Teva Pharmaceuticals
- DESIGNATION – Regulatory Affairs Associate
- DEPARTMENT – Regulatory Affairs
- CATEGORY – Regulatory Submission Management
- EXPERIENCE – Freshers & Experienced
Regulatory Affairs Associate Job Responsibilities
- Handle document-level publishing responsibilities and address formatting or technical errors.
- Ensure quality assurance for agency-compliant submissions.
- Familiar with ICH standards and regulator requirements for submission in eCTD, NeeS, and paper formats.
- Experience with publishing post approval submission and ensuring compliance with regulatory guidelines.
- Coordinate with scientific personnel to ensure adherence to internal and external publishing standards.
- Stay updated about evolving publishing standards both within the organization and across global regulatory bodies.
- Basic Knowledge of tools commonly utilized in regulatory publishing, such as Global Insight, Veeva Vault, ISI Toolbox, Adobe Acrobat, and Lorenz Validator, is required.
Who can apply for this job role?
- Bachelor’s or Master’s degree in Pharmacy (B.Pharm / M.Pharm)
- Master’s degree in Life Sciences (M.Sc)
- Minimum 01 year of working experience in regulatory publishing in the EU or US market is required.
Skills Required
- Expertise in eCTD publishing tools such as GlobalSubmit / Insight Publisher / Lorenz docuBridge.
- Experience with Document Management Systems such as Veeva Vault and Documentum.
- Skilled in regulatory submission formats (eCTD / NeeS and Paper)
- Analytical & Problem-Solving Skills
- Clear verbal and written communication to coordinate with stakeholders.
Teva Pharmaceuticals Regulatory Affairs Associate Salary
The salary package details have not been disclosed yet by Teva Pharmaceutical Industries Limited for the job role of Regulatory Affairs Associate, but as per the industry standard and job profile, the expected annual salary may range between INR 03 LPA to INR 05 LPA.
Job Details
The candidates for the role of Regulatory Affairs Associate will be recruited for full-time services at Teva Pharmaceutical Industries Limited. You can check out the details of the job location, nature of the job, and whether the job is remote-based or office-based by reviewing the article.
- Job Location – Navi Mumbai, Maharashtra, India
- Contract Type – Full-Time
- Work Type – Onsite
- Industry Type – Pharmaceuticals
How to Apply for the Teva Pharmaceuticals Regulatory Affairs Associate Job?
To apply for the job, candidates can click on the link shared below and fill in all the details specified in the application form along with the updated resume containing the details of their qualifications and experience.
Click on the shared link to apply and submit the application before the deadline. and shortlisted Candidates will receive an email from the HR department for further updates.
