Latest Pharma Jobs in Mumbai – Apply for Regulatory Affairs Jobs at Teva Pharmaceuticals

Teva Pharmaceuticals is inviting skilled life science professionals to apply for the role of Regulatory Affairs Associate I in Navi Mumbai, India. This opportunity is ideal for M.Sc. Life Sciences graduates with 1–3 years of experience in pharmaceutical regulatory affairs. Join one of the world’s top generic medicine producers and help shape US labeling submissions and regulatory documentation in a fast-paced, impact-driven environment.

About the Company:

Teva Pharmaceuticals is the world’s leading manufacturer of generic medicines, committed to improving global health by making medications more affordable and accessible. Operating in nearly 60 countries, Teva helps over 200 million people daily. The company’s diverse workforce drives innovation across essential medicine portfolios, including products listed by the World Health Organization. With a global presence and a commitment to inclusive growth, Teva offers a dynamic platform for professionals to thrive and contribute to better healthcare.

Job Details

Job Posting: Regulatory Affairs Associate I

Location: Navi Mumbai, India, 400706

Job ID: 62820

Job Description:

The RA Associate I, under direct supervision, is responsible for the preparation and revision of high-quality US Gx labeling documents filed under an ANDA and/or 505(b)2, if required, while ensuring adherence to federal regulations and meeting deadlines driven by company goals.

Key Responsibilities for Latest Pharma Jobs:

• Develop and QC US labeling documents for ANDA and 505(b)(2) submissions.

• Create and validate SPLs aligned with FDA drug listing requirements.

• Prepare side-by-side comparisons and submission packages for the FDA.

• Ensure submission documents meet eCTD formatting and quality expectations.

• Stay current on FDA regulations and labeling guidelines.

• Perform proofreading using TVT and maintain high document accuracy.

• Collaborate cross-functionally and manage deadlines efficiently.

Required Qualifications:

• Bachelor’s or Master’s in pharma, with 2-3 Years in the Pharmaceutical Industry.

• 1–3 years of experience in regulatory affairs, specifically US labeling.

• Proficiency in Microsoft Office, Adobe Acrobat Pro, and familiarity with eCTD.

• Strong attention to detail, multitasking, and communication skills.

• Hands-on experience with TVT (preferred).

If you’re looking to grow in regulatory affairs with a leading global pharmaceutical company, this is your chance to make an impact in healthcare.

APPLY ONLINE HERE

Keywords: Regulatory Affairs, Teva Pharmaceuticals, Latest Pharma Jobs, Navi Mumbai, India, Pharmaceutical Industry, FDA Regulations