Regulatory Affairs Job at Teva Pharmaceuticals | Pharmacy Graduates Apply Now
Teva Pharmaceuticals, the world’s leading manufacturer of generic medicines, is seeking a motivated Regulatory Affairs Associate I to support regulatory activities across International Markets. This Regulatory Affairs Job is ideal for individuals with 2–3 years of pharma experience who want to grow their expertise in global regulatory operations, compliance, and documentation within a high-impact, mission-driven organization.
- Job Title: Regulatory Affairs Associate I
- Location: Bangalore, India, 560064
- Job Id: 64000
Teva Pharmaceuticals
Teva Pharmaceutical Industries Ltd. is one of the world’s largest and most trusted generics and specialty medicine companies, delivering affordable and high-quality healthcare solutions to millions of patients globally. Headquartered in Israel, Teva has a strong legacy of over a century in developing generics, complex generics, biosimilars, and specialty medicines across central nervous system, respiratory, oncology, and pain management fields. With extensive R&D capabilities, a global manufacturing network, and a commitment to improving access to essential treatments, Teva continues to play a pivotal role in shaping the future of cost-effective and innovative healthcare worldwide.
Responsibilities of the Pharmacy Job
- Completion of designated projects and tasks supporting International Market RA, according to internal Work Instructions, with guidance and direction by the manager and more senior colleagues.
- Maintaining related documentation and regulatory IT systems, in line with internal procedures.
- Timely task completion in line with Work Instructions, with accurate tracker updates and adherence to compliance standards.
- Communication with Teva units across International Markets, with 3rd Parties and with related Health Authorities.
- Fulfilling other allocated department duties and ad-hoc tasks as directed by senior regulatory affairs staff.
- Completion of trainings assigned in Teva internal learning management system within defined timeframes.
- Attending team meetings and providing regular updates on the assigned activities and tasks to the manager and/or to senior regulatory affairs staff.
- Maintaining and developing awareness of the current/pending regulatory legislation and guidelines.
Experience and Qualifications of the Pharmacy Job
Qualification:
- Masters in Pharmacy
- College or University degree or equivalent work experience that provide knowledge of and exposure to fundamental theories, principles and concepts.
Experience:
- 2-3 years of experience in the Pharmaceutical Industry, ideally within Regulatory Affairs but R&D, Development or QA would be considered.
- Experience of regulatory documentation within Europe and/or International Markets.
Knowledge
- Work experience involving core regulatory concepts and procedures.
- Ability to use existing internal procedures to solve routine or standard problems.
- Proficient in regulatory IT systems to support compliance and documentation processes.
- Working knowledge of Office-365 applications and Veeva Vault systems.
- Strong focus on Compliance and regulatory standards.
- Basic knowledge of project management principles and tools.
- Strong organizational skills to meet self, team and company goals.
- Ability to identify a problem or need for decision that exceeds the competence of the individual.
- French and/or German language proficiency will be an added advantage.
