Join Teva Pharmaceuticals For Regulatory Affairs Jobs in Navi Mumbai | Apply Now
Looking to build your future in Regulatory Affairs Jobs with a trusted global brand? Teva Pharmaceuticals Careers now offers an excellent opportunity for skilled professionals as a Regulatory Affairs Associate II in Navi Mumbai. This role is ideal for candidates seeking M Pharm jobs, who want to expand their expertise in FDA submissions, compliance, and post-approval processes. Join Teva Pharmaceuticals one of the world’s leaders in affordable healthcare and make a real difference in the pharmaceutical industry.
Job Details:
- Job Title: Regulatory Affairs Associate II
- Location: Navi Mumbai, India, 400706
- Job Id: 64918
About The Company:
Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to making healthcare more affordable and accessible. With operations in nearly 60 countries, Teva serves over 200 million people daily, providing trusted medicines that are part of the WHO Essential Medicines List. Working at Teva Pharmaceuticals Careers means joining a diverse, innovative, and inclusive environment where every employee contributes to better health outcomes worldwide.
Job Description For the Regulatory Affairs job
The Regulatory Affairs Associate II at Teva Pharmaceuticals plays a key role in preparing, reviewing, and submitting high-quality regulatory documents to the FDA, ensuring compliance with global regulatory standards. This is a great opportunity for those pursuing M Pharm Jobs and wanting to develop hands-on expertise in post-approval submissions and regulatory operations within a world-class pharma organization.
Key Responsibilities
- Maintain approved applications in compliance with FDA regulations for assigned ANDA Annual Reports.
- Independently compile and publish annual reports and simple supplements for management review.
- Support management with complex supplements for experience development.
- Evaluate post-approval change controls for accuracy and compliance.
- Update and maintain regulatory databases and trackers in real time.
- Train junior staff (Associate I) on internal procedures and documentation.
- Perform additional projects and regulatory tasks as assigned.
Qualifications: Ideal for Regulatory Affairs Jobs
- Education: M.Pharm degree in Regulatory Affairs or Quality Assurance preferred.
- Experience: Minimum of 4 years in the pharmaceutical industry (Regulatory, QA, Analytical, Laboratory, or Production).
Skills:
- Strong organizational and multitasking abilities.
- Proficient in MS Word, Excel, and online research.
- Excellent communication and writing skills.
- Ability to work both independently and collaboratively.
Why Choose This Company?
- Work with a global healthcare leader trusted by millions.
- Advance your career in Regulatory Affairs Jobs and M Pharm Jobs.
- Gain valuable exposure to international regulatory frameworks and FDA submissions.
- Be part of a diverse, innovative, and inclusive environment that values growth and collaboration.
Equal Opportunity Commitment
Teva Pharmaceuticals is committed to diversity, inclusion, and equal employment opportunities. The company prohibits discrimination based on age, race, gender, religion, disability, or any protected status. All hiring practices ensure accessibility and fairness for every applicant.
