Regulatory Affairs Specialist

We are looking for a skilled Regulatory Affairs Specialist to join our team at Medifodil Smart Pharma Solutions, with 4-7 years of experience in the Pharmaceutical & Life Sciences industry.

• Develop and implement regulatory strategies to ensure compliance with relevant laws and regulations.
• Prepare and review regulatory submissions, including applications, reports, and other documents.
• Collaborate with cross-functional teams to ensure timely and accurate submission of regulatory documents.
• Conduct thorough reviews of regulatory requirements and develop solutions to meet them.
• Maintain up-to-date knowledge of changing regulatory requirements and implement necessary changes.
• Provide guidance and support to internal stakeholders on regulatory matters.

• Strong understanding of pharmaceutical and life sciences regulations and laws.
• Excellent analytical and problem-solving skills, with attention to detail and ability to work under pressure.
• Effective communication and collaboration skills, with the ability to work with diverse stakeholders.
• Ability to prioritize tasks and manage multiple projects simultaneously.
• Strong organizational and time management skills, with the ability to meet deadlines.
• Familiarity with regulatory software and systems, and the ability to learn new systems quickly.