Teva Pharmaceuticals is inviting applications for the role of Regulatory Affairs Specialist II in Navi Mumbai, India. This opportunity is ideal for professionals seeking growth in pharma jobs, especially within Regulatory Affairs Specialist II roles focused on global regulatory publishing and eCTD submissions.
At Teva, you will contribute to high-impact regulatory operations supporting EU, US, and Canada markets while working in a globally recognized pharmaceutical environment.
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in pharma jobs and biopharmaceutical innovation. The company focuses on delivering high-quality medicines and advancing regulatory excellence across international markets. This Regulatory Affairs Specialist II Teva job offers exposure to global regulatory systems and lifecycle management processes.
Key Responsibilities โ Regulatory Affairs Specialist II Teva
As a Regulatory Affairs Specialist II, you will be responsible for:
- Publishing and dispatching complex eCTD submissions for EU, US, and Canada markets
- Handling post-approval regulatory submissions and lifecycle management activities
- Performing document-level publishing and quality control checks
- Ensuring compliance with regulatory guidelines for Regulatory Affairs Specialist II pharma jobs
- Collaborating with cross-functional scientific and regulatory teams
- Working with tools like Veeva Vault, Adobe Acrobat, Global Insight, and Lorenz Validator
- Maintaining accuracy, timelines, and compliance in all submissions
Required Qualifications
To apply for this Teva Regulatory Affairs Specialist II job, candidates should have:
- B.Pharm with minimum 2 years experience in Regulatory Affairs
- OR M.Pharm / Master of Life Sciences with 0โ1 year experience
- Strong understanding of eCTD, NeeS, and regulatory submission standards
- Knowledge of ICH guidelines and global regulatory frameworks
- Experience with regulatory IT systems used in pharma jobs
- Excellent written and spoken English communication skills
- Ability to work in a global, culturally diverse environment
Benefits of Working at Teva
Joining Teva in this Regulatory Affairs Specialist II role provides:
- Global exposure to regulatory submission projects
- Career growth in high-demand pharma jobs
- Flexible work culture and learning opportunities
- Health and wellness support programs
- Internal mobility and skill development through dedicated platforms
- Inclusive and collaborative workplace environment
Salary Package
Expected salary for Regulatory Affairs Specialist II Teva jobs:
โน6 โ โน12 LPA (Approx.) depending on experience and skills
How to Apply
