Teva Pharmaceuticalsย is a global leader inย generic and specialty medicines, committed to makingย healthcare more affordable and accessible. With a presence inย nearly 60 countries, Teva produces many medicines listed on theย WHO Essential Medicines List, impacting overย 200 million patients daily. The company fosters aย diverse, inclusive workplaceย 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:
- Manageย regulatory lifecycleย forย Tevaโs 3rd party client (Medis) dossiersย inย Europe & international markets.
- Ensureย regulatory documentsย are updated and compliant with procedures.
- Prepare and submitย variationsย to regulatory authorities or clients.
- Trackย submission timelines, approvals, and deficiencies.
- Communicate regulatory updates toย internal & external stakeholders.
- Maintainย regulatory databasesย and provideย status reports to management.
- Work onย specialized regulatory projectsย as assigned.
Skills & Competencies:
โ Strong organizational & communication skills
โ Proficient in English (written & verbal)
โ Strategic thinking & adaptability
โ Team player with proactive attitude
โ Good computer skills
Eligibility & Qualifications
- Education:ย M Pharm / MSc in a relevant field
- Experience:ย 0-1 years inย Regulatory Affairs (Pharma)
- Preferred Skills:ย Knowledge ofย regulatory submissions, variations, and compliance
Benefits & Work Culture
โ
Global exposure in a leading pharmaceutical company
โ
Inclusive & diverse workplace
โ
Career growth opportunities
โ
Professional development programs
โ
Equal employment opportunity (EEO compliant)
How to Apply
