Regulatory Affairs Associate III – Teva Pharma, WALK IN

With operations in nearly 60 countries, Teva is one of the world’s leading manufacturers of generic medicines and innovative treatments. Each day, over 200 million people benefit from Teva’s therapies. Joining Teva means being part of a mission to make quality healthcare accessible globally.

⚙️ Key Responsibilities

As a Regulatory Affairs Associate III, you will:

• Maintain approved applications in compliance with FDA regulations for assigned ANDA Annual Reports.
• Independently prepare, review, and submit high-quality regulatory submissions to the US FDA.
• Handle change control assessments and ensure completeness and accuracy before progression.
• Compile and publish Annual Reports, Supplements (CBE-0, CBE-30, PAS), and Post-Approval Submissions.
• Train junior team members (Associates I & II) on regulatory procedures, databases, and internal processes.
• Ensure timely updates of internal regulatory databases and trackers.
• Participate in process improvement initiatives to enhance submission quality and efficiency.

🎓 Qualifications and Experience

• Education: M.Pharm degree (Regulatory Affairs or Quality Assurance preferred).
• Experience: Minimum 5+ years in the pharmaceutical industry (Regulatory, Analytical, QA, or Production).
• Strong understanding of ICH and FDA guidelines.
• Proven ability to evaluate regulatory documents and determine appropriate action.
• Excellent written and verbal communication skills.
• Highly organized, detail-oriented, and able to multitask.
• Strong critical and logical thinking capabilities.

💼 Why Join Teva?

• Work with a global pharmaceutical leader known for innovation and integrity.
• Opportunity to lead and mentor junior associates.
• Exposure to US Post-Approval Regulatory operations.
• Inclusive, diverse, and collaborative work environment.
• Competitive compensation and benefits package.

🗓️ Walk-in Recruitment Drive Details

📅 Date: Saturday, 11th October 2025
🕙 Time: 10:00 AM – 2:00 PM
📍 Location: Teva Pharmaceuticals, Seawoods, Navi Mumbai
💼 Work Location: Navi Mumbai, India

Teva is looking for candidates with 4–10 years of experience in:

• Change Control Assessment for the US market
• Post-Approval activities – Annual Reports, CBE-0, CBE-30, PAS

✨ To register for the drive, click the official registration link or scan the QR code shared in Teva’s post.

📋 How to Apply

Application Link