Regulatory Affairs Associate I – Fresher / Early-Career Opportunity
Location: Bangalore, India – 560064
Category: Regulatory Affairs / International Markets / Pharmaceutical Compliance
Job Type: Full-Time
Experience Required: Fresher / 0–2 Years
Job ID: 64000
Company Overview
Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to making healthcare more affordable and accessible. With operations across nearly 60 countries, Teva reaches over 200 million patients daily and produces numerous medicines listed on the World Health Organization’s Essential Medicines List.
This is an excellent opportunity for freshers or early-career professionals to gain hands-on experience in international regulatory affairs, global pharmaceutical compliance, and regulatory documentation processes.
Position Overview
The Regulatory Affairs Associate I will provide support to Teva’s International Markets Regulatory Affairs (RA) team. This role is ideal for early-career candidates or freshers looking to start a career in regulatory affairs, offering exposure to global regulatory submissions, documentation, and compliance standards.
You will work under guidance from managers and senior colleagues, assisting in tasks critical to maintaining regulatory compliance and supporting product registration in international markets.
Key Responsibilities
Assist in executing assigned regulatory projects and tasks according to internal Work Instructions (WIs).
Support maintenance of documentation and regulatory IT systems in compliance with company procedures.
Ensure timely and accurate completion of tasks, updating trackers and adhering to regulatory standards.
Communicate with Teva units across International Markets, third parties, and relevant health authorities.
Support senior regulatory affairs staff with ad-hoc tasks and departmental duties.
Complete assigned training modules in Teva’s learning management system within defined timelines.
Attend team meetings and provide regular updates on assigned activities.
Maintain awareness of current and upcoming international regulatory legislation, guidelines, and best practices.
Qualifications & Experience
Educational Requirements:
Master’s in Pharmacy (MPharm) or Master’s in Science/Life Sciences.
College or university degree with foundational knowledge in pharmaceutical sciences or life sciences.
Experience:
Fresher / 0–2 years of experience in the pharmaceutical industry is acceptable.
Previous exposure to regulatory affairs, R&D, development, or quality assurance (QA) is a plus.
Familiarity with regulatory documentation for European or international markets is advantageous.
Skills & Competencies:
Basic understanding of regulatory affairs concepts and procedures.
Proficiency in regulatory IT systems, compliance tools, and Office-365 applications; familiarity with Veeva Vault is a plus.
Strong organizational and project management skills.
Excellent communication skills and ability to work in a cross-functional, global team environment.
Knowledge of French and/or German is an added advantage.
Strong focus on compliance and adherence to regulatory standards.
Why Join Teva?
Launch your career in regulatory affairs with hands-on exposure to global markets.
Gain knowledge of international regulatory frameworks, compliance, and pharmaceutical documentation.
Work in a collaborative, global environment alongside industry experts.
Opportunity to develop your career in a fast-growing, innovative pharmaceutical company.
Equal Employment Opportunity
Teva Pharmaceuticals is committed to equal opportunity in employment. Employment decisions are made without regard to age, race, color, religion, sex, disability, sexual orientation, gender identity, veteran status, or any other legally protected status. Candidates requiring accommodations during the recruitment process will be supported fully.
Apply Now: Start your career in Regulatory Affairs – International Markets with Teva Pharmaceuticals, and gain critical experience in global compliance, regulatory documentation, and pharmaceutical operations.
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