Teva Pharma Hiring for Regulatory Affairs Associate
Teva Pharmaceuticals, one of the world’s most respected and trusted pharmaceutical companies, is inviting applications for the position of Regulatory Affairs Associate I at its Navi Mumbai facility. This opportunity is ideal for professionals with 2–3 years of experience in post-approval regulatory affairs who are passionate about contributing to the pharmaceutical industry’s global compliance and innovation efforts. Teva Pharma Hiring for Regulatory Affairs Associate
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in the production of generic and specialty medicines, operating in over 60 countries and serving millions of patients worldwide. With a strong focus on quality, safety, and affordability, Teva continues to play a crucial role in making healthcare accessible to all. The company’s regulatory affairs division is responsible for ensuring that all medicines meet global health and safety standards, particularly within regulated markets like the European Union. Teva Pharma Hiring for Regulatory Affairs Associate
Position Details – Regulatory Affairs Associate I
Position: Regulatory Affairs Associate I
Company: Teva Pharmaceuticals
Qualification: M.Pharm or M.Sc. in Life Sciences, Pharmaceutical Sciences, or a related discipline
Experience: 2–3 years of experience in Post-Approval Regulatory Affairs
Location: Navi Mumbai, Maharashtra, India
Employment Type: Full-time, On-site
Industry: Pharmaceuticals
Salary (Estimated): INR 5.0 – 7.5 LPA (depending on qualifications and experience)
Key Responsibilities
As a Regulatory Affairs Associate I at Teva Pharmaceuticals, you will play a vital role in managing regulatory submissions and maintaining compliance across various European markets. Your key responsibilities will include: Teva Pharma Hiring for Regulatory Affairs Associate
- Preparing, compiling, and submitting post-approval regulatory submissions as per European Union (EU) legislation.
- Reviewing and ensuring high-quality regulatory documentation in compliance with Teva’s internal standards and external regulatory requirements.
- Monitoring regulatory submissions, ensuring timely follow-ups, and securing approvals within designated timelines.
- Maintaining updated records of registration documentation and regulatory databases.
- Supporting marketing authorization (MA) compliance and variation management activities.
- Coordinating with European regulatory agencies and internal Teva departments for submission-related queries and lifecycle management.
- Staying informed about evolving EU regulatory frameworks, variations, and compliance updates.
- Providing regulatory guidance and support to internal departments including quality assurance, manufacturing, and project management teams.
Eligibility Criteria and Qualifications
Educational Qualification:
- M.Pharm or M.Sc. degree in Life Sciences, Pharmaceutical Sciences, or a closely related field.
Experience Required:
- 2–3 years of experience in post-approval regulatory affairs, preferably in the European markets (EU region).
- Experience with dossier submissions, MA renewals, and variation procedures is highly desirable.
Skills and Competencies:
- Strong understanding of EU regulatory procedures, CTD/eCTD submission formats, and lifecycle management.
- Excellent written and verbal communication skills for effective documentation and correspondence.
- Proficiency in MS Office applications and regulatory databases.
- Strong analytical, organizational, and time management skills.
- Ability to work collaboratively in cross-functional teams and meet strict deadlines.
- High attention to detail and accuracy in documentation.
Why Join Teva Pharmaceuticals?
Teva Pharmaceuticals offers an excellent platform for growth, learning, and professional advancement. As a Regulatory Affairs Associate, you will have the opportunity to work with a globally recognized organization and gain hands-on experience in the European regulatory environment. Teva Pharma Hiring for Regulatory Affairs Associate
Here are some key reasons to join Teva:
- Work with one of the largest pharmaceutical manufacturers in the world.
- Exposure to international regulatory submissions and post-approval lifecycle management.
- Collaborative and inclusive work culture focused on innovation and career development.
- Opportunities for skill enhancement and cross-functional learning.
- Contribute to a global mission of improving healthcare accessibility and compliance.
- Teva Pharma Hiring for Regulatory Affairs Associate
Job Location
- City: Navi Mumbai, Maharashtra, India
- Pincode: 400706
- Work Mode: Full-time, On-site
Salary and Benefits
- Estimated Salary Range: INR 5.0 – 7.5 LPA
- Competitive salary package based on experience, qualifications, and interview performance.
- Comprehensive employee benefits, including health insurance, paid leaves, and performance-based incentives.
- Teva Pharma Hiring for Regulatory Affairs Associate
How to Apply
Interested and eligible candidates can apply online through the official Teva Pharmaceuticals career portal. Candidates are advised to ensure that their resumes are updated with relevant experience and qualifications before applying.
Conclusion
If you have a background in Regulatory Affairs and are looking for a career opportunity with a global pharmaceutical leader, Teva Pharmaceuticals in Navi Mumbai offers an excellent position to grow professionally. With exposure to European market submissions and a dynamic regulatory environment, this role will strengthen your expertise and open doors to long-term career advancement in the pharmaceutical industry. Teva Pharma Hiring for Regulatory Affairs Associate
Apply today and take the next step in your regulatory affairs career with Teva Pharmaceuticals.
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