EXECUTIVE REGULATORY AFFAIRS

You should have a Masters or Bachelors degree in Science / Pharmacy along with at least 7-10 years of experience in a similar function within the pharmaceutical industry. As a Regulatory Affairs professional, you must have supported regulatory affairs functions on finished dosage forms. It is essential to possess a sound and deep knowledge of current Regulatory / GMP requirements including US FDA, EU GMP, and PIC/s. Your role will require strong initiative skills, enabling you to work both independently and as part of a team. Proficiency in English communication is vital for effective coordination within the organization and with external stakeholders. Additionally, you should have advanced Microsoft Office skills, particularly in Word, Excel, PowerPoint, and Outlook. This position offers opportunities to leverage your expertise in regulatory affairs and contribute to the continued success of our pharmaceutical operations in Hyderabad, India and Nanjing, China.,