Regulatory Affairs Intern - Miami, Florida
About The Position
Accelerating answers Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Beckman Coulter Life Sciences, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Bec LS means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Beckman Life Sciences you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Regulatory Affairs Intern will gain hands-on experienc e in regulatory strategy, documentation, and compliance within the life sciences industry. You’ll work alongside experienced professionals to support regulatory submissions and ensure alignment with global standards. This position reports to the Senior Manager, Regulatory Affairs and is part of the Flow Cytometry business located in Miami and will be an on-site role.
Requirements
- Currently pursuing a bachelor’s or master’s degree in Regulatory Affairs, Life Sciences, Pharmacy, Public Health, or a related discipline
- Strong attention to detail and organizational skills
- Excellent written and verbal communication abilities
- Familiarity with regulatory terminology and documentation practices
- Strong verbal and written communication skills.
- Ability to work independently and in a team environment
Nice To Haves
- Prior internship or coursework in regulatory affairs or quality assurance
- Understanding of FDA, EMA, or ICH guidelines
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint
Responsibilities
- Assist in the preparation, review, and submission of regulatory documents to health authorities
- Support regulatory tracking systems and maintain documentation databases
- Conduct research on regulatory requirements and industry guidelines
- Collaborate with cross-functional teams including R&D, Quality, and Clinical Affairs
- Help ensure compliance with applicable regulations, standards, and company policies
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What This Job Offers
Career Level
Intern
Number of Employees
5,001-10,000 employees
