STeva 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
