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 experience 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.
What will you do:
· 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
Who are you:
· 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
It would be a plus if you also possess previous experience in:
· 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
The hourly range for this role is $30.00. This is the rate that we in good faith believe is the rate of compensation for this role at the time of this posting
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
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We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.