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Regulatory Affairs Associate I

Teva Pharmaceuticals
Teva Pharmaceuticals
2 years
preferred by company
10 Feb. 11, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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


Regulatory Affairs Associate I – ANDA Annual Reports & 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.


Role Overview

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


Key Responsibilities

Regulatory Submissions & FDA 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.

Change Control & Documentation Review

  • 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.

Regulatory Data Management

  • 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.

Additional Responsibilities

  • 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.


Required Experience

  • 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.


Educational Qualifications

  • 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.


Technical & Functional Skills

  • 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.


Work Environment

  • 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.


Career Growth Opportunities

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


About Teva Pharmaceuticals

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.


Apply via ThePharmaDaily.com

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.