Teva Pharmaceuticals Hiring Regulatory Affairs Associate III in Navi Mumbai USFDA submissions regulatory jobs India 2026 apply experienced professionals now.
Teva Pharmaceuticals has announced a new opportunity for experienced regulatory professionals with openings for the role of Regulatory Affairs Associate III at its Navi Mumbai location. This role is ideal for candidates with strong experience in US regulatory submissions, particularly those familiar with ANDA lifecycle management and FDA compliance requirements.
Professionals with a background in regulatory affairs and experience handling post-approval submissions, supplements, and annual reports can explore this opportunity. The role offers exposure to global regulatory frameworks and the chance to work with one of the world’s leading generic pharmaceutical companies. Teva Pharmaceuticals Hiring Regulatory Affairs Associate III
Company Overview
Teva Pharmaceuticals is a global biopharmaceutical company known for its leadership in generic medicines and specialty drug development. The organization operates across multiple therapeutic areas, including neuroscience and immunology, while maintaining a strong presence in the global generics market.
With operations spanning several countries, Teva offers professionals opportunities to work in collaborative, innovation-driven environments focused on delivering affordable and high-quality medicines worldwide. Teva Pharmaceuticals Hiring Regulatory Affairs Associate III
Job Location & Employment Type
- Location: Navi Mumbai, India
- Employment Type: Full-time
- Department: Regulatory Affairs
- Job ID: 64203
This role is suited for experienced regulatory professionals focusing on US market submissions.
Job Role Overview
The Regulatory Affairs Associate III will be responsible for preparing and managing regulatory submissions in compliance with USFDA guidelines. The role involves handling post-approval submissions, evaluating change controls, and supporting regulatory lifecycle management for approved products.
This position requires strong technical knowledge of regulatory documentation and the ability to manage submissions with minimal supervision.
Key Roles & Responsibilities
Regulatory Submissions
- Preparing and reviewing regulatory submissions aligned with FDA requirements
- Managing annual reports for approved ANDA applications
- Compiling and publishing supplements for regulatory review
- Supporting post-approval submission strategies
Change Control Evaluation
- Reviewing change controls related to post-approval changes
- Ensuring completeness and accuracy of documentation
- Progressing submissions after internal approvals
Lifecycle Management
- Maintaining regulatory compliance of approved applications
- Monitoring regulatory trackers and databases
- Supporting submission timelines and quality deliverables
Training & Process Support
- Assisting in training junior regulatory associates
- Supporting process improvements and knowledge sharing
- Contributing to regulatory workflow enhancements
This role demands strong documentation skills and a proactive regulatory approach. Teva Pharmaceuticals Hiring Regulatory Affairs Associate III
Eligibility Criteria
Educational Qualification
Candidates must hold relevant qualifications such as:
- B.Pharm or M.Pharm
- M.Sc in Life Sciences
- Other pharmacy or science-related degrees
Candidates with advanced regulatory education may have an advantage.
Experience
- Minimum 6+ years of regulatory affairs experience
- Strong exposure to US regulatory markets preferred
- Experience handling FDA submissions and ANDA lifecycle management
Candidates with hands-on USFDA submission experience are highly preferred.
Skills Required
- Strong understanding of ICH and FDA guidelines
- Ability to evaluate regulatory documentation independently
- Excellent written and verbal communication skills
- Strong organizational and multitasking abilities
- Analytical and logical thinking skills
- Attention to detail in regulatory documentation
Candidates with strong regulatory writing and review capabilities will excel in this role. Teva Pharmaceuticals Hiring Regulatory Affairs Associate III
Salary & Benefits
- Compensation will be as per company norms and experience level
- Opportunity to work with a global pharmaceutical leader
- Exposure to US regulatory frameworks
- Structured career growth opportunities
- Learning and development programs
- Employee benefits and wellness support
Teva offers strong career progression within global regulatory functions.
Selection Process
The hiring process may include:
- Resume screening based on regulatory experience
- Technical interview focusing on USFDA submissions
- Final HR or leadership discussion
Candidates with direct ANDA lifecycle experience may be prioritized.
How to Apply
Interested candidates can apply through the official Teva careers portal by searching: Teva Pharmaceuticals Hiring Regulatory Affairs Associate III
Role: Regulatory Affairs Associate III
Location: Navi Mumbai
Job ID: 64203
Ensure your resume highlights:
- USFDA submission experience
- ANDA lifecycle exposure
- Regulatory documentation expertise
- Process improvement contributions
Early applications are recommended due to limited openings.
Important Dates
- Application Mode: Online application
- Hiring Type: Ongoing recruitment
Candidates are advised to apply early for better shortlisting chances.
Why Apply for This Pharma Job?
Regulatory affairs roles in global pharmaceutical companies offer strong long-term career growth and international exposure. This opportunity at Teva allows professionals to work directly on US regulatory submissions, which are highly valued across the pharmaceutical industry.
Experience in ANDA lifecycle management and FDA compliance can open doors to senior regulatory leadership roles, global submission management positions, and cross-regional regulatory careers. Teva Pharmaceuticals Hiring Regulatory Affairs Associate III
For professionals aiming to build expertise in international regulatory affairs, this role offers a strong platform within a globally recognized pharmaceutical organization. Teva Pharmaceuticals Hiring Regulatory Affairs Associate III
Important Note
IndiaPharmaJobs.in is an independent pharmaceutical job information platform and is not affiliated with Teva Pharmaceuticals. We do not participate in the recruitment process. Applicants should apply through the official careers portal and verify job details independently before proceeding. Teva Pharmaceuticals Hiring Regulatory Affairs Associate III
Final Words
If you are an experienced regulatory affairs professional with strong USFDA submission experience, this opportunity at Teva Pharmaceuticals is worth exploring. The Regulatory Affairs Associate III role offers exposure to ANDA lifecycle management, post-approval submissions, and global regulatory environments. Apply early and ensure your resume highlights relevant US regulatory expertise for better shortlisting chances. Teva Pharmaceuticals Hiring Regulatory Affairs Associate III
