Paid Regulatory Affairs Internship in USA
Looking to break into regulatory science at a world-class biotech company? This paid regulatory affairs internship in Miami, Florida offers a rare chance to gain hands-on experience with Beckman Coulter careers, a global leader under the Danaher umbrella. Designed as an internship opportunity for life science graduates, this on-site internship in USA places you at the heart of regulatory strategy, compliance, and innovation in life sciences and diagnostics.
About Beckman Coulter Life Sciences
Beckman Coulter Life Sciences, one of Danaher’s 15+ operating companies, is dedicated to accelerating answers in life sciences, diagnostics, and biotechnology. The organization supports customers engaged in life-saving work, from fundamental biological research to the development of vaccines, medicines, and cell and gene therapies. The company fosters a culture of belonging where diverse perspectives are valued, and innovation is driven through the Danaher Business System of continuous improvement. Beckman Coulter Life Sciences operates at the forefront of transforming human health by delivering solutions that truly matter.
Internship Details:
- Intern Title: Regulatory Affairs Intern
- Company: Beckman Coulter Life Sciences
- Location: Miami, Florida, United States of America
- Category: Internship
- Job ID: R1295247
- Work Location Type: On-site
Regulatory Affairs Intern Position Overview
The Regulatory Affairs Intern role provides hands-on experience in regulatory strategy, documentation, and compliance within the life sciences industry. The intern will work closely with experienced regulatory professionals to support regulatory submissions and ensure alignment with global regulatory standards.
This position reports to the Senior Manager, Regulatory Affairs and is part of the Flow Cytometry business. The role is based on-site in Miami, Florida.
Key Responsibilities of Paid Regulatory Affairs Internship
- Assist with 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 Research & Development, Quality, and Clinical Affairs
- Support compliance with applicable regulations, standards, and internal company policies
Required Qualifications
- Currently pursuing a Bachelor’s or Master’s degree in Regulatory Affairs, Life Sciences, or a related discipline
- Strong attention to detail and organizational skills
- Excellent written and verbal communication abilities
- Familiarity with regulatory terminology and documentation practices
- Ability to work both independently and collaboratively in a team environment
Preferred QualificationsÂ
- Prior internship experience or coursework in regulatory affairs or quality assurance
- Understanding of FDA, EMA, or ICH guidelines
- Proficiency in Microsoft Office applications (Word, Excel, PowerPoint)
Compensation
The hourly pay rate for this role is $30.00, representing the company’s good-faith estimate of compensation at the time of posting.
