Teva Pharmaceuticals Hiring Regulatory Affairs Associate (labeling)

Regulatory Affairs Associate I Opportunity at Teva Pharmaceuticals – BPharm/MPharm Graduates in Navi Mumbai

Hiring Regulatory Affairs Associate I in Navi Mumbai for BPharm/MPharm/MSc graduates with 1–3 years experience in pharma labeling. Apply now at Teva Pharmaceuticals.

Regulatory Affairs Associate I Job Opening for Pharmacy Graduates at Teva Pharmaceuticals, Navi Mumbai

If you’re a BPharm, MPharm, or MSc Life Sciences graduate with a passion for regulatory compliance, this is your chance to join Teva Pharmaceuticals, a global leader in generic medicines. The Regulatory Affairs Associate I position is now open at the Navi Mumbai location. This role is ideal for professionals with 1 to 3 years of experience in US Gx labeling and Structured Product Labeling (SPL).

About Teva Pharmaceuticals

Teva is committed to making good health more affordable and accessible worldwide. With operations in nearly 60 countries and millions relying on their medications daily, Teva leads in generic drug manufacturing and maintains a strong presence on the WHO’s Essential Medicines List.

Position: Regulatory Affairs Associate I (Labeling)

Work Location:

Teva Pharmaceuticals, Navi Mumbai, Maharashtra, India – 400706

Key Responsibilities:

• Prepare and revise high-quality US Gx labeling documents under ANDA and 505(b)(2) submissions.
• Develop compliant Structured Product Labeling (SPL) files and ensure complete drug listing information.
• Conduct proofreading, QC, and formatting of regulatory documents.
• Compile full FDA submission responses, including side-by-side comparisons and labeling materials.
• Coordinate with Regulatory Operations and use publishing software for eCTD-compliant submissions.
• Stay up to date with US FDA labeling regulations and Teva SOPs.

Required Qualifications:

• BPharmacy/MPharmacy/MSc in Life Sciences
• 1 to 3 years of experience in Regulatory Affairs, preferably in labeling.
• Experience with SPL development and eCTD submission formats.

Preferred Candidate Profile:

• In-depth knowledge of FDA regulatory requirements
• Experience with electronic submission tools and proofreading systems
• Team-oriented with excellent communication skills

How to Apply:

Interested candidates can apply directly through Teva’s official career portal: 👉 Apply Now

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