Are you a driven and detail-oriented individual looking to jumpstart your career in the dynamic field of regulatory affairs? Look no further than Philips! We are seeking an ambitious and enthusiastic Intern-Regulatory Affairs to join our team and gain hands-on experience in navigating the complex world of healthcare regulations. As an intern in our Regulatory Affairs department, you will have the opportunity to work closely with our experienced team and contribute to the development and compliance of our innovative medical devices. We are looking for a motivated self-starter with a strong interest in regulatory affairs and a passion for making a positive impact in the healthcare industry. If you are ready to take on new challenges and grow your skills in a fast-paced and supportive environment, we welcome you to apply for this exciting opportunity at Philips.
- Assist the Regulatory Affairs team in ensuring compliance with all relevant laws, regulations, and standards in the healthcare industry.
- Conduct research and analysis on current and upcoming regulatory requirements for medical devices.
- Prepare and submit regulatory submissions to relevant agencies and authorities.
- Review and maintain documentation for regulatory compliance, including product labeling and technical files.
- Collaborate with cross-functional teams to provide regulatory guidance and support for product development and launch.
- Participate in meetings and discussions with regulatory agencies to ensure a thorough understanding of regulations and to address any issues or concerns.
- Stay up-to-date on changes and updates in regulations and communicate any potential impact to the team.
- Assist in conducting internal audits and inspections to ensure compliance with regulations and company standards.
- Contribute to the development and implementation of processes and procedures to streamline and improve regulatory processes.
- Maintain accurate and organized records of all regulatory documents and submissions.
- Communicate effectively with team members and stakeholders, providing updates and progress on projects and tasks.
- Demonstrate a strong commitment to quality and patient safety in all regulatory activities.
- Continuously seek opportunities for learning and growth in the field of regulatory affairs.
- Adhere to company policies and procedures, as well as regulatory requirements at all times.
Bachelor's Degree In A Related Field Such As Regulatory Affairs, Biology, Chemistry, Or Healthcare Administration.
Strong Understanding Of Regulatory Guidelines And Requirements For Medical Devices And Pharmaceuticals.
Excellent Communication And Interpersonal Skills To Effectively Collaborate With Cross-Functional Teams And Regulatory Agencies.
Proficiency In Regulatory Software And Databases, As Well As Experience With Document Management And Submission Processes.
Prior Internship Or Work Experience In A Regulatory Affairs Role, Preferably Within The Medical Device Or Pharmaceutical Industry.
Quality Assurance
Communication Skills
Project Management
Data Analysis
Technical Writing
Risk assessment
Regulatory compliance
Team collaboration
FDA regulations
Problem-Solving
Medical Devices
Research Abilities
Communication
Conflict Resolution
Leadership
Time management
creativity
Critical thinking
Teamwork
Adaptability
Problem-Solving
Empathy
According to JobzMall, the average salary range for a Intern-Regulatory Affairs in Orlando, FL, USA is $45,000 - $65,000 per year. This range can vary depending on the specific company, industry, and level of experience of the intern.
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Royal Philips is a health technology company focused on improving people's health and enabling better outcomes across the health continuum from healthy living and prevention, to diagnosis, treatment and home care. Philips leverages advanced technology and deep clinical and consumer insights to deliver integrated solutions. The company is a leader in diagnostic imaging, image-guided therapy, patient monitoring and health informatics, as well as in consumer health and home care.

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