Apply for Teva Pharma Hiring for Regulatory Affairs Associate I in Navi Mumbai. Explore pharma regulatory jobs and global compliance careers.
Introduction
Teva Pharmaceuticals, one of the world’s largest and most trusted pharmaceutical companies, is inviting applications for the position of Regulatory Affairs Associate I in Navi Mumbai, India. This is a remarkable opportunity for professionals who are passionate about regulatory affairs, data management, and global compliance in the pharmaceutical industry. Teva Pharma Hiring for Regulatory Affairs Associate I
Teva Pharmaceuticals is recognized globally as a pioneer in generic medicines and innovative healthcare solutions. The company is committed to making quality and affordable medicines accessible to millions of people around the world. This role provides a unique opportunity to contribute directly to regulatory data integrity, ensuring that Teva continues to meet international compliance standards and deliver safe, effective medicines to patients across the globe. Teva Pharma Hiring for Regulatory Affairs Associate I
If you are a detail-oriented professional with a background in life sciences or information technology, this could be the ideal next step in your pharmaceutical career. Teva Pharma Hiring for Regulatory Affairs Associate I
About Teva Pharmaceuticals
Founded over a century ago, Teva Pharmaceuticals is a global leader in generic, specialty, and over-the-counter medicines. With operations in more than 60 countries, Teva provides affordable and high-quality healthcare solutions to over 200 million people every day. Teva Pharma Hiring for Regulatory Affairs Associate I
Teva’s mission is to improve health and make quality medicines accessible to more people globally. The company combines scientific innovation with advanced technology to support regulatory compliance, research, and patient safety.
The Navi Mumbai office plays a vital role in Teva’s global operations, particularly in the areas of regulatory data management, product registration, and global compliance. The Regulatory Affairs Associate position is integral to ensuring that Teva’s global portfolio adheres to ever-evolving international regulatory requirements. Teva Pharma Hiring for Regulatory Affairs Associate I
Position Overview: Regulatory Affairs Associate I
The Regulatory Affairs Associate I position at Teva Pharmaceuticals focuses on regulatory data management, data analytics, and compliance operations. The successful candidate will ensure that product registration data and related documentation meet global regulatory standards. Teva Pharma Hiring for Regulatory Affairs Associate I
The role demands accuracy, analytical thinking, and a solid understanding of pharmaceutical regulatory processes. The associate will collaborate with global teams to execute data management tasks, ensure quality control, and support system integration projects. Teva Pharma Hiring for Regulatory Affairs Associate I
Key Responsibilities
As a Regulatory Affairs Associate I, your day-to-day responsibilities will include:
- Regulatory Data Management:
Maintain and manage Teva’s global regulatory data to ensure full compliance with xEVMPD and Article 57 requirements. - Data Analytics Operations:
Execute regulatory data analytics and reporting operations as per established Standard Operating Procedures (SOPs) and global quality standards. - Quality Control and Data Integrity:
Perform rigorous data integrity checks and quality control (QC) reviews for entries in Teva’s Global Registration database to maintain accuracy and reliability. - Documentation and Data Extraction:
Extract and maintain regulatory data from dossiers, submission documents, and internal systems, ensuring timely updates and consistency across all records. - Cross-functional Collaboration:
Work closely with cross-functional teams within Global Regulatory Affairs (GRA) to align on compliance objectives and contribute to strategic data initiatives. - System and Process Improvement:
Support ongoing projects aimed at improving regulatory data quality, optimizing systems, and integrating new compliance tools and platforms.
Required Qualifications
Educational Background
- Required: Bachelor’s or Master’s degree in Life Sciences or Information Technology.
- Preferred: Advanced degree (MS or equivalent) in a scientific or IT discipline.
Experience
- Required: 1–3 years of professional experience, preferably in regulatory operations, regulatory affairs, or data management within the pharmaceutical industry.
- Preferred: Prior experience working with Regulatory Information Management (RIM) systems or product registration data.
Core Skills and Competencies
- Strong understanding of pharmaceutical regulatory processes and global compliance requirements.
- Ability to manage and analyze large sets of regulatory data accurately.
- Excellent attention to detail and commitment to data quality.
- Proficiency in using regulatory or document management systems.
- Strong collaboration and communication skills to work effectively across departments.
- Analytical mindset with a focus on process improvement and efficiency.
Preferred Attributes
- Experience working in a multinational pharmaceutical environment.
- Understanding of electronic submission standards and global registration databases.
- Familiarity with data integrity principles and regulatory data validation.
- Enthusiasm for learning new technologies and contributing to system enhancement projects.
- Ability to prioritize multiple tasks and deliver high-quality results under deadlines.
Why Join Teva Pharmaceuticals
Working at Teva Pharmaceuticals is more than just a job—it’s an opportunity to make a lasting impact on global health. Teva Pharma Hiring for Regulatory Affairs Associate I
Here’s why Teva stands out as an employer of choice:
- Global Leadership: Be part of a company that leads the world in generic and specialty medicines, serving millions of patients daily.
- Career Growth: Gain exposure to global regulatory operations and build expertise in pharma data analytics and compliance.
- Inclusive Culture: Work in a diverse, supportive, and collaborative environment that values innovation and teamwork.
- Learning & Development: Access continuous professional development, mentoring, and global career opportunities.
- Social Impact: Contribute to a mission that enhances healthcare accessibility and improves lives worldwide.
- Work-Life Balance: Teva promotes flexibility, wellbeing, and a culture of respect for employees across all levels.
Work Environment
This role is based in Navi Mumbai, one of Teva’s strategic hubs for regulatory operations in India. The work culture encourages collaboration, innovation, and continuous improvement. Teva Pharma Hiring for Regulatory Affairs Associate I
Employees in this position will interact with global teams across different time zones, contributing to international projects and regulatory submissions.
Teva supports both on-site and hybrid working models, offering flexibility while maintaining strong team connections and productivity.
How to Apply
Interested candidates can apply online for the Regulatory Affairs Associate I position through Teva Pharmaceuticals’ official career portal. Teva Pharma Hiring for Regulatory Affairs Associate I
Step-by-Step Application Process:
- Visit the official Teva Pharmaceuticals Careers page: https://careers.teva (or search “Teva Careers India” on Google).
- In the search bar, enter the Job Title: Regulatory Affairs Associate I.
- Select Location: Navi Mumbai, India.
- Click on the job listing titled Regulatory Affairs Associate I – Navi Mumbai.
- Review the job description carefully and ensure you meet the required qualifications.
- Click “Apply Now” and create or log in to your candidate profile.
- Complete the online application form and upload your latest resume (CV).
- Submit your application before the deadline to ensure consideration.
Important Dates
- Published On: November 6, 2025
- Last Date to Apply: Open until position is filled (early application encouraged)
Conclusion
The Regulatory Affairs Associate I role at Teva Pharmaceuticals offers a fantastic opportunity to develop your career in global regulatory operations. With its focus on compliance, data accuracy, and teamwork, this position is ideal for professionals seeking growth in the pharmaceutical industry. Teva Pharma Hiring for Regulatory Affairs Associate I
By joining Teva, you become part of a global organization dedicated to improving healthcare access, ensuring regulatory excellence, and driving medical innovation.
If you are passionate about contributing to meaningful work and building a long-term career in regulatory affairs, this is your chance to make an impact. Teva Pharma Hiring for Regulatory Affairs Associate I
Apply today and become a part of Teva’s global journey toward better health for all.
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