Do you want to be a driving force in a rapidly expanding environment, making a tangible difference in the process? Our Client a global leading Healthcare company is looking for a Senior Regulatory Affairs Manager Tasks Support regulatory activities for products before and after launch. Keep records and databases organized and up to date. Make sure projects run smoothly and report progress to management. Join meetings for product launches, quality, and safety. Update technical files and review them regularly. Organize monthly calls with teams and share updates with management. Help with QA and safety matters and communicate clearly with the team. Manage 1-2 team members in the regulatory department. Attend training to improve skills. Respond to regulatory agencies on time. Profile A degree in a relevant field, recognized in the EU, with experience in pharmaceutical regulations. At least 7 years of experience in the generic pharmaceutical industry. Good knowledge of how pharmaceutical products are developed. Experience working with different dosage forms like immediate, modified, and extended release. Familiar with ICH and regulatory guidelines. Comfortable using Microsoft Office and other basic IT tools. Please contact me on or please call me on 49 30 726211428 for further information.