Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to making healthcare more affordable and accessible. With a presence in nearly 60 countries, Teva produces many medicines listed on the WHO Essential Medicines List, impacting over 200 million patients daily. The company fosters a diverse, inclusive workplace with opportunities for professional growth.
Detailed Job Description
Job Title: Regulatory Affairs Specialist II
Location: Navi Mumbai, India
Job ID: 62655
Experience: 0-1 years
Qualification: M Pharm / MSc
Key Responsibilities:
- Manage regulatory lifecycle for Teva’s 3rd party client (Medis) dossiers in Europe & international markets.
- Ensure regulatory documents are updated and compliant with procedures.
- Prepare and submit variations to regulatory authorities or clients.
- Track submission timelines, approvals, and deficiencies.
- Communicate regulatory updates to internal & external stakeholders.
- Maintain regulatory databases and provide status reports to management.
- Work on specialized regulatory projects as assigned.
Skills & Competencies:
✔ Strong organizational & communication skills
✔ Proficient in English (written & verbal)
✔ Strategic thinking & adaptability
✔ Team player with proactive attitude
✔ Good computer skills
Eligibility & Qualifications
- Education: M Pharm / MSc in a relevant field
- Experience: 0-1 years in Regulatory Affairs (Pharma)
- Preferred Skills: Knowledge of regulatory submissions, variations, and compliance
Benefits & Work Culture
✅ Global exposure in a leading pharmaceutical company
✅ Inclusive & diverse workplace
✅ Career growth opportunities
✅ Professional development programs
✅ Equal employment opportunity (EEO compliant)
How to Apply
