Job Title: Regulatory Affairs Associate I
Location: Navi Mumbai, India (400706)
Company: Teva Pharmaceuticals
Job ID: 65574
Employment Type: Full-Time
Industry: Regulatory Affairs | Pharmaceuticals | Generics | FDA Submissions
Teva Pharmaceuticals is seeking a detail-oriented Regulatory Affairs Associate I to join its Regulatory Affairs team in Navi Mumbai, India. This role is ideal for professionals with foundational experience in regulatory affairs, quality control, R&D, or pharmaceutical manufacturing who are looking to build expertise in FDA regulatory submissions and ANDA lifecycle management.
Teva is a leading global biopharmaceutical company with a strong generics portfolio, committed to delivering high-quality medicines worldwide while advancing innovation in key therapeutic areas.
The Regulatory Affairs Associate I will support the preparation and maintenance of regulatory submissions, with a primary focus on ANDA Annual Reports and FDA compliance activities. Working under direct supervision, the role involves document review, change control evaluation, regulatory database management, and regulatory submission preparation in accordance with FDA guidelines.
This position is well suited for candidates seeking to grow in:
US FDA Regulatory Affairs
ANDA Lifecycle Management
Change Control Review & Documentation
Regulatory Submission Preparation
Pharmaceutical Quality & Compliance
Prepare and submit ANDA Annual Reports in compliance with FDA regulations.
Assist in preparing supplements and amendments for FDA submissions as experience progresses.
Maintain approved applications in alignment with US regulatory requirements.
Support regulatory documentation for post-approval changes.
Review supporting documents related to change controls, including:
Batch records
Analytical methods
Specifications
Manufacturing documentation
Conduct side-by-side comparisons to evaluate the accuracy and appropriateness of proposed changes.
Assist in filing determinations in accordance with applicable FDA regulations and guidance.
Accurately populate and maintain regulatory databases and trackers in real time.
Ensure data accuracy and timely updates for internal regulatory systems.
Support cross-functional teams by maintaining up-to-date submission records.
Participate in assigned regulatory projects and process improvement initiatives.
Stay updated on FDA regulations and guidance relevant to assigned products.
Collaborate with QA, QC, R&D, and Production teams to ensure regulatory compliance.
Minimum 2 years of experience in Regulatory Affairs, or relevant experience in:
Analytical / Quality Control
Research & Development (R&D)
Pharmaceutical Manufacturing / Production
Experience within the pharmaceutical or biotechnology industry is mandatory.
Exposure to FDA regulatory submissions or ANDA lifecycle management is preferred.
Bachelor’s or Master’s degree in Pharmacy (M.Pharm preferred, especially in Regulatory Affairs or Quality Assurance).
Equivalent pharmaceutical industry experience may be considered.
Basic knowledge of US FDA regulations and ANDA submission processes.
Strong understanding of pharmaceutical change control documentation.
Proficiency in Microsoft Office (Word, Excel, Outlook).
Ability to manage multiple tasks and changing priorities.
Strong attention to detail and documentation accuracy.
Good verbal and written communication skills.
Ability to work both independently and within cross-functional teams.
Office-based role in Navi Mumbai, India.
Exposure to global regulatory submission processes.
Collaborative work culture within a multinational pharmaceutical organization.
Opportunity to gain hands-on experience in US FDA compliance and generics lifecycle management.
This role offers career development in:
US Regulatory Affairs (FDA)
Post-Approval Change Management
ANDA Strategy & Lifecycle Management
Regulatory Compliance & Documentation
Potential progression paths include:
Regulatory Affairs Associate II
Regulatory Affairs Specialist
Senior Regulatory Affairs Executive
Regulatory Affairs Manager
Teva is a global leader in generics and innovative medicines, committed to improving patient access to high-quality treatments worldwide. The company fosters an inclusive, high-performing culture that encourages professional growth and collaboration.
If you are a Regulatory Affairs professional with 2+ years of pharmaceutical industry experience, this opportunity in Navi Mumbai offers valuable exposure to US FDA submissions and ANDA lifecycle management.
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