Regulatory Affairs Associate I job vacancies at TEVA Pharmaceuticals
Are you an experienced regulatory affairs professional looking to make a difference in the pharmaceutical industry? If so, TEVA Pharmaceuticals has an exciting opportunity for you. As a Regulatory Affairs Associate I, you will be responsible for ensuring compliance with EU legislation and in-house standards while prioritizing, planning, and monitoring submissions for designated projects.
Location: Navi Mumbai, India, 400706
Company: Teva Pharmaceuticals
Job Id: 47626
Preparing High-Quality Submissions
Your primary responsibility will be to prepare, compile, review, and submit high-quality submissions for all required post-approval activities. You will be expected to maintain registration documentation and associated electronic databases by in-house procedures.
Compliance with Legislation and Business Needs
As a Regulatory Affairs Associate I, you will be responsible for ensuring compliance with both legislation and business needs. You will work closely with internal and external customers, stakeholders, and TEVA project teams to provide regulatory support.
Professional Communication and Status Updates
Professional communication with other Teva departments across Europe and European Agencies regarding proposed and pending submissions are key. You will also be responsible for providing regular status updates of ongoing work and activities to superiors or managers.
Awareness of Current Regulatory Legislation and Guidelines
In addition, it is important to maintain and develop an awareness of current and pending regulatory legislation and guidelines. As such, you will be expected to stay up-to-date with industry trends and developments.
To qualify for this position, you should have one to three years of overall pharmaceutical industry experience, preferably in the regulatory affairs department. A degree in science, life sciences, pharmacy, or equivalent qualifications is also required.
Join TEVA Pharmaceuticals
At TEVA Pharmaceuticals, we are committed to delivering high-quality and affordable medicines to patients around the world. As a Regulatory Affairs Associate I, you will be an essential part of our team, helping us achieve our mission.