Apply for Regulatory Affairs Associate II Job at Teva Pharma in Navi Mumbai. Join Teva’s Regulatory Data Analytics global team today.
Company: Teva Pharmaceuticals
Position: Regulatory Affairs Associate II – Regulatory Data Analytics (RDA)
Location: Seawoods, Navi Mumbai, Maharashtra
Qualification: Bachelor’s or Master’s Degree in Life Sciences or Information Technology
Experience: 2–5 years
Application Mode: Online / Email Application
Job Status: Verified Job
About Teva Pharmaceuticals
Teva Pharmaceuticals is one of the world’s largest and most trusted pharmaceutical companies, renowned for its leadership in generic medicines, specialty products, and biopharmaceutical innovation. With a mission to improve the health and well-being of millions of people every day, Teva operates across more than 60 countries, delivering affordable, high-quality medicines that impact over 200 million patients globally. Regulatory Affairs Associate II Job at Teva Pharma
Teva’s commitment to quality, innovation, and regulatory compliance ensures that every product meets the highest standards of safety and efficacy. As part of its continuous focus on operational excellence, the company’s Global Regulatory Operations (GRO) division plays a critical role in ensuring data integrity and compliance across worldwide regulatory submissions. Regulatory Affairs Associate II Job at Teva Pharma
About the Role – Regulatory Affairs Associate II (Regulatory Data Analytics)
Teva Pharmaceuticals is inviting applications for the position of Regulatory Affairs Associate II within its Regulatory Data Analytics (RDA) team located in Seawoods, Navi Mumbai. This role offers an exciting opportunity to work at the intersection of regulatory operations and data analytics, supporting the company’s mission to ensure compliance and quality across global markets. Regulatory Affairs Associate II Job at Teva Pharma
As a Regulatory Affairs Associate II, you will contribute to the management, analysis, and validation of regulatory data, ensuring that all submissions align with international compliance requirements, including Article 57 and xEVMPD (Extended EudraVigilance Medicinal Product Dictionary) standards. Regulatory Affairs Associate II Job at Teva Pharma
You will also collaborate with cross-functional teams to maintain data accuracy and integrity, support compliance initiatives, and drive improvements in regulatory information management systems. Regulatory Affairs Associate II Job at Teva Pharma
Key Responsibilities
In this role, you will be responsible for a range of regulatory and analytical tasks that ensure Teva’s data-driven regulatory processes operate efficiently and accurately. Your key responsibilities will include: Regulatory Affairs Associate II Job at Teva Pharma
- Executing Regulatory Data Analytics (RDA) operations in accordance with company Standard Operating Procedures (SOPs) and Work Instructions.
- Managing and maintaining global registration data across Teva’s regulatory systems to ensure alignment with internal frameworks and global standards.
- Performing quality control (QC) reviews and conducting data integrity checks to guarantee the accuracy and completeness of regulatory data.
- Interpreting and extracting information from regulatory dossiers with precision and domain-specific understanding.
- Collaborating closely with global and regional regulatory teams to enhance data consistency and compliance across markets.
- Supporting ongoing data projects focused on improving regulatory data integration, quality, and accessibility.
- Identifying opportunities for process optimization and contributing to the continuous improvement of regulatory data governance systems.
- Mentoring and supporting junior team members in regulatory data analytics tasks, ensuring knowledge sharing and adherence to best practices.
Qualifications and Experience
Educational Requirements:
- Required: Bachelor’s or Master’s Degree in Life Sciences or Information Technology.
- Preferred: Master’s in a Scientific or Information Technology discipline (such as Biotechnology, Bioinformatics, or Regulatory Informatics).
Experience Requirements:
- Required: 2–5 years of experience in Regulatory Affairs, Regulatory Operations, or Data Management within the pharmaceutical industry.
- Hands-on experience with xEVMPD, Article 57 compliance, or similar regulatory databases is highly preferred.
- Prior exposure to global regulatory submissions, electronic document management systems, and data analytics tools is an advantage.
Technical & Professional Skills:
- Strong analytical mindset with attention to detail and data accuracy.
- Understanding of global regulatory frameworks and compliance requirements.
- Proficiency in Microsoft Excel, data visualization tools, and regulatory information systems.
- Excellent communication and teamwork skills with the ability to collaborate across global teams.
- Strong problem-solving capabilities with the initiative to improve processes and systems.
About the Department – Global Regulatory Operations (GRO) Data Analytics
The Global Regulatory Operations Data Analytics (GRO RDA) team at Teva plays an integral role in managing product registration data, ensuring that all regulatory information is accurate, up to date, and compliant with international regulations. Regulatory Affairs Associate II Job at Teva Pharma
The team focuses on maintaining data integrity, ensuring Article 57 compliance, and facilitating accurate xEVMPD submissions for Teva’s extensive global product portfolio. By leveraging advanced data analytics and governance frameworks, the RDA team supports smarter, faster, and more compliant decision-making within the organization. Regulatory Affairs Associate II Job at Teva Pharma
Why Join Teva Pharmaceuticals?
Joining Teva Pharmaceuticals means becoming part of a dynamic, inclusive, and globally recognized organization where your expertise can make a lasting difference. Here are some reasons why this opportunity is ideal for professionals looking to grow in the regulatory field: Regulatory Affairs Associate II Job at Teva Pharma
- Global Impact: Contribute to regulatory operations that directly influence patient safety and healthcare compliance across multiple countries.
- Innovative Environment: Work in a data-driven environment that leverages cutting-edge analytics tools and regulatory technologies.
- Career Growth: Teva offers clear career progression paths with ongoing learning opportunities and exposure to global regulatory projects.
- Collaborative Culture: Be part of a supportive, cross-functional team that values diversity, integrity, and scientific excellence.
- Competitive Compensation: Receive an attractive salary and comprehensive benefits package in line with industry standards.
- Work-Life Balance: Teva encourages a healthy balance between professional and personal commitments, with flexibility where possible.
Location Details
- Work Location: Seawoods, Navi Mumbai, Maharashtra, India – 400706
- Job Type: Full-time, On-site
The Seawoods office is a key Teva facility supporting multiple global regulatory operations. Employees benefit from a modern workspace designed for collaboration, continuous learning, and innovation. Regulatory Affairs Associate II Job at Teva Pharma
How to Apply
If you are passionate about regulatory data analytics and wish to advance your career in a globally respected organization, Teva Pharmaceuticals invites you to apply for this position.
Interested candidates can share their updated resumes directly via email to:
Email ID: Rekha.Rathod@teva.co.in
Alternatively, you can also apply online through the official Teva Pharmaceuticals career portal.
Job Summary
| Particulars | Details |
|---|---|
| Company | Teva Pharmaceuticals |
| Position | Regulatory Affairs Associate II – Regulatory Data Analytics |
| Qualification | Bachelor’s or Master’s Degree in Life Sciences or Information Technology |
| Experience | 2–5 years |
| Location | Seawoods, Navi Mumbai, Maharashtra |
| Job Type | Full Time |
| Application Mode | Online / Email |
| Industry Type | Pharmaceuticals / Regulatory Affairs |
| Status | Verified Job |
About Teva’s Commitment to Diversity and Innovation
At Teva, inclusion and diversity are central to innovation. The company fosters an environment where professionals from different backgrounds collaborate to create impactful healthcare solutions. Teva’s mission—to be a global leader in providing accessible and quality medicines—is supported by a culture of integrity, transparency, and scientific rigor. Regulatory Affairs Associate II Job at Teva Pharma
Teva Pharmaceuticals continuously invests in regulatory technology and analytics to improve compliance efficiency, reduce risks, and accelerate approvals, ensuring that patients have timely access to safe and effective medicines worldwide.
Final Thoughts
The position of Regulatory Affairs Associate II – Regulatory Data Analytics at Teva Pharmaceuticals represents an excellent opportunity for professionals passionate about combining life sciences expertise with data analytics and regulatory compliance.
By joining Teva, you will contribute to a purpose-driven organization that enhances global health outcomes while offering you a platform for continuous professional growth and global exposure. Regulatory Affairs Associate II Job at Teva Pharma
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