Regulatory Affairs Associate I Vacancy at Teva Pharmaceuticals
- M.Pharm Regulatory Affairs Associate Openings at Teva Navi Mumbai
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Major Challenges
- Eligibility / Qualifications
- Location & Salary
- Application Process
- FAQs
- What qualification is required?
- How much experience is needed?
- Does the role involve document management?
- Will I work with global teams?
- Is this an administrative-heavy role?
- Summary Table
M.Pharm Regulatory Affairs Associate Openings at Teva Navi Mumbai
Apply for Regulatory Affairs Associate I openings at Teva Navi Mumbai for M.Pharm graduates with 2–4 years experience.
Teva Pharmaceuticals is hiring experienced Regulatory Affairs professionals for its UK/IE Regulatory Affairs division in Navi Mumbai. The role suits candidates who can manage end-to-end lifecycle activities, maintain regulatory documentation, update information systems, and support submissions for UK/IE markets. This is an opportunity to work with one of the world’s most trusted generics manufacturers and contribute to regulatory compliance for high-impact global medicines.
Company Overview
Teva Pharmaceuticals is a global leader in generic medicines, serving over 200 million patients daily. With operations across nearly 60 countries, the company develops safe, effective, and affordable therapies that support public health worldwide. Teva’s regulatory teams play a critical role in maintaining compliance for essential medicines, supporting new product registrations, managing marketing authorisations, and ensuring high-quality documentation across international markets.
Job Role & Responsibilities
In this role, you will support UK/IE Regulatory Affairs with administrative and regulatory lifecycle tasks. The position requires coordination with multiple internal teams, strong documentation skills, and the ability to manage changing priorities.
Key Responsibilities
- Provide administrative and regulatory support for Marketing Authorisation lifecycle management
- Maintain tracking tools, regulatory systems, and databases with accurate updates
- Monitor team inboxes and ensure timely communication handling
- Prepare, update, and manage Product Information within Teva’s Document Management System
- Generate and submit simple variations or label/leaflet updates for UK/IE licensed products
- Provide UK/IE-specific documentation for EU RA submissions and variations
- Maintain electronic files in accordance with Teva internal procedures
- Identify process improvement opportunities and escalate where required
- Update regulatory information systems following changes or approvals
- Support UK/IE RA projects involving documentation requests
- Proofread mock-ups to ensure regulatory and compliance accuracy
- Provide ad hoc administrative support to cross-functional teams
- Support cancellation processes per internal guidelines
Major Challenges
- Managing deadlines while navigating frequent changes in priorities
- Coordinating with diverse internal and external stakeholders
- Maintaining accuracy in documentation while handling multiple tasks
Eligibility / Qualifications
- M. Pharma degree in RA/QA discipline, a plus.
- Minimum of two years Regulatory Affairs experience and/or analytical/QC, R&D/laboratory or production experience in pharmaceutical/biotech industry.
- Basic computer skills such as Word, Excel and familiarity with internet
- Ability to work independently and on teams
- Good verbal and written communication skills
- Must be well organized, detail oriented, have the ability to multi-task and manage changing priorities.
Location & Salary
- Location: Navi Mumbai, Maharashtra, India (400706)
- Salary: Competitive, based on experience, regulatory expertise, and organisational guidelines
Application Process
Candidates can apply directly through the Teva Pharmaceuticals careers portal.
Apply here: https://careers.teva/job/Navi-Mumbai-Regulatory-Affairs-Associate-I-Indi-400706/1351408400/
Ensure your resume reflects experience in regulatory lifecycle management, documentation control, and UK/IE regulatory processes.
FAQs
What qualification is required?
M.Pharm is mandatory.
How much experience is needed?
2–4 years in Regulatory Affairs or related pharmaceutical operations.
Does the role involve document management?
Yes. You will manage Product Information, regulatory files, and submission documentation.
Will I work with global teams?
Yes. The role involves coordination with UK/IE and EU Regulatory Affairs.
Is this an administrative-heavy role?
It combines administrative tasks with regulatory support and lifecycle activities.
Summary Table
| Category | Details |
|---|---|
| Company | Teva Pharmaceuticals, Navi Mumbai |
| Vacancies | Regulatory Affairs Associate I |
| Required Education | M.Pharm |
| Experience | 2–4 years in Regulatory Affairs or pharmaceutical operations |
To apply for this job please visit careers.teva.
