Regulatory Affairs Job at Teva Pharmaceuticals | M Pharmacy Graduates | Apply Now
Looking for a rewarding Regulatory Affairs Job in the pharmaceutical industry? This Pharma Job at Teva Pharmaceuticals in Navi Mumbai gives you the chance to prepare FDA submissions, annual reports, and change control evaluations while advancing your career in a supportive and collaborative environment.
- Job Position: Regulatory Affairs Associate
- Location: Navi Mumbai, India, 400706
- Job ID: 66857
About the Company
Teva Pharmaceuticals is a global leader in innovative biopharmaceuticals with a world-class generics business. Teva supports neuroscience, immunology, and high-quality medicine delivery worldwide, fostering an inclusive culture that values fresh thinking, personal growth, and work-life balance.
Job Description
Teva Pharmaceuticals is hiring for a Regulatory Affairs Job role. Under supervision, the Associate will prepare FDA submissions, supplements, amendments, and annual reports. Responsibilities include assisting in change control evaluations and maintaining regulatory databases. This Pharma Job offers exposure to global regulatory affairs and professional growth in a collaborative setting.
Key Responsibilities
- Prepare FDA regulatory submissions, supplements, amendments, and annual reports under supervision.
- Review documents supporting change controls for accuracy and quality.
- Maintain regulatory databases and trackers in real time.
- Support ANDA annual report submissions and maintain compliance.
- Assist in other regulatory projects as assigned.
Qualifications
- M. Pharma degree in the RA/QA discipline preferred.
- Minimum 2 years of experience in Regulatory Affairs or related analytical/QC, R&D, lab, or production roles in pharma/biotech.
- Proficient in Word, Excel, and internet usage.
- Strong verbal and written communication skills.
- Organized, detail-oriented, capable of multitasking, and able to work independently or in teams.
Why Join This Role?
This Regulatory Affairs Job at Teva Pharmaceuticals offers a great Pharma Job opportunity to work with a global biopharmaceutical leader while gaining hands-on experience in FDA submissions, regulatory compliance, and annual report preparation. You will be part of a collaborative team that supports career growth, learning opportunities, and a positive work environment.
