Teva Pharmaceuticals, a global leader in generic medicines and essential healthcare products, is hiring a Regulatory Affairs Associate I for its Navi Mumbai location. This opportunity is ideal for M.Pharm professionals with 2–4 years of regulatory affairs experience who want to work on UK and Ireland (UK/IE) regulatory portfolios & US Post Approval in a multinational pharmaceutical environment.
At Teva, professionals contribute to making healthcare more affordable and accessible worldwide, supporting products used daily by over 200 million people. This role offers strong exposure to marketing authorisation lifecycle management, regulatory submissions, and cross-functional collaboration.
Key Responsibilities – Regulatory Affairs Associate I
- Provide full administrative support to the UK/IE Regulatory Affairs team
- Manage lifecycle activities of Marketing Authorisations (MAs)
- Prepare, manage, and update Product Information in Teva’s Document Management System
- Generate and submit simple variations and label/leaflet updates for approved UK/IE products
- Support EU Regulatory Affairs with UK/IE-specific documentation
- Maintain regulatory tracking tools, databases, and electronic files as per SOPs
- Update regulatory information systems accurately and on time
- Proofread artwork mock-ups to ensure regulatory compliance
- Support licence cancellations as per internal procedures
- Monitor team inboxes and manage ad-hoc regulatory documentation requests
- Identify and escalate process improvement opportunities
Major Job Challenges
- Managing multiple priorities with frequent unscheduled requests
- Meeting strict regulatory timelines
- Coordinating with diverse internal and external stakeholders
- Maintaining accuracy and compliance under pressure
Qualifications & Experience Required
Education
- Bachelor’s or Master’s in Pharmacy / Master’s in Science / Life Sciences
Experience
- 2–4 years of experience in a pharmaceutical regulatory affairs or related function
Regulatory Knowledge
- Basic understanding of pharmaceutical company processes
- Familiarity with regulatory documentation and lifecycle management
- Exposure to UK, IE, or EU regulatory systems is an advantage
Required Skills
- Strong written and verbal communication skills
- Excellent time management and organisational abilities
- Ability to work independently and within cross-functional teams
- Proficiency in Microsoft Word, Excel, and Outlook
- High attention to detail and compliance mindset
- Ability to work under pressure and meet tight deadlines
Key Stakeholder Interaction
Internal
- UK/IE Regulatory Affairs
- EU Regulatory Affairs
- Manufacturing, QA, QC, and Supply Chain
- Medical Affairs, Pharmacovigilance, and Medical Information
- Commercial, Portfolio, and Marketing teams
- Regulatory Information Management & Artwork teams
External
- MHRA, HPRA
- Business partners, suppliers, and customers
Salary & Benefits (Indicative)
- Salary Range: ₹6,00,000 – ₹9,00,000 per annum (INR)
- Exposure to global regulatory markets (UK/IE & EU)
- Career growth within a leading multinational pharma company
- Inclusive, diverse, and equal-opportunity work environment
- Structured learning and process-driven culture
How to Apply
📩 Interested candidates can share their updated CVs at:
apeksha.shinde01@teva.co.in
