Teva Pharmaceutical Industries Ltd Walk-in On 11th Oct 2025

• Who we are

The opportunity

The Associate III, with minimal to no guidance, prepares, reviews and submits high quality regulatory submissions to the FDA within company timelines and in accordance with regulatory guidelines. The Associate III will be responsible for independently evaluating change controls (intended for post approval changes), will assure the CC is complete and accurate and in the absence of any comments will progress the CC accordingly. In addition, he/she will monitor any/all Regulatory or team databases and trackers and will proactively and accurately update them when changes are required. Annual Reports, supplements, post approval submissions and assisting management with the training of regulatory staff will be the primary responsibilities of the Associate III.  

How you’ll spend your day

Maintain approved applications in compliance with FDA regulations for assigned ANDA Annual reports.

Independently and proactively request documentation required for annual reports, compile, finalize and publish for managements review and subsequent dispatch to the Agency

Independently work on supplements, compile and publish for managements review. Take a proactive approach for more complex submissions and contact internal stakeholders (when needed) to gain further insight on any given supplement. Convey findings to management and incorporate any.all applicable information in the submission to ensure a quality and a right first time submission.

Assist management and proactively train Associate I’s and Associate II’s on guidance’s, internal processes, procedures, databases and trackers 

Other projects and duties as required/assigned.

Process improvement

Your experience and qualifications

M. Pharma degree in RA/QA discipline, a plus.

Minimum 5+ years pharmaceutical industry experience; Regulatory, Analytical, QA, laboratory or production experience preferred.

Demonstrates an understanding of ICH and FDA guidelines

Demonstrates the ability to evaluate regulatory documents and determine appropriate action.

Demonstrates excellent verbal and written communication skills.

Demonstrates excellent organization skills and the ability to multi-task; detail oriented.

Possesses strong critical and logical thinking.

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on “Employee Central”. By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment