Regulatory Affairs Internship at Beckman Coulter
Beckman Coulter Life Sciences is seeking a Regulatory Affairs Intern for its Flow Cytometry business in Miami, Florida. This full-time, on-site regulatory affairs internship at Beckman Coulter Careers offers hands-on exposure to regulatory strategy, documentation, and compliance within the life sciences and biotechnology industry. The role offers students an excellent opportunity to gain practical experience while supporting global regulatory submissions and compliance initiatives.
Internship Details:
- Job Title: Regulatory Affairs Intern
- Job Requisition ID: R1295247
- Location: Miami, Florida, United States
- Employment Type: Full Time (Internship)
- Work Model: On-site
- Business Unit: Flow Cytometry
- Reports To: Senior Manager, Regulatory Affairs
- Hourly Pay: $30.00 per hour
About the Company:
Beckman Coulter Life Sciences, a Danaher operating company, is a global leader in life sciences, diagnostics, and biotechnology solutions. The company supports customers engaged in critical research areas such as vaccine development, cell and gene therapy, and biological discovery. Powered by the Danaher Business System, Beckman Coulter fosters continuous improvement, innovation, and a culture where science-driven impact saves lives worldwide.
Educational Requirements for the Regulatory Affairs Internship:
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Currently pursuing a Bachelor’s or Master’s degree in Regulatory Affairs, Life Sciences, Pharmacy, Public Health, or a related discipline
Key Responsibilities of the Regulatory Affairs Intern:
- In this Internship at Beckman Coulter Careers, you have to 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, standards, and industry guidelines
- Collaborate with cross-functional teams, including R&D, Quality, and Clinical Affairs
- Support regulatory compliance with applicable regulations and company policies
Skills Required for the Regulatory Affairs Intern Role:
- Strong attention to detail and organizational skills
- Excellent written and verbal communication abilities
- Familiarity with regulatory terminology and documentation practices
- Ability to work independently and collaboratively in a team environment
- Basic understanding of FDA, EMA, or ICH guidelines (preferred)
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) preferred
- Prior coursework or internship experience in Regulatory Affairs or Quality Assurance is a plus
Benefits of the Regulatory Affairs Internship:
- Competitive hourly compensation
- Hands-on regulatory affairs experience in the life sciences industry
- Exposure to global regulatory standards and submissions
- Opportunity to work with experienced regulatory professionals
- Collaborative, inclusive, and innovation-driven work culture
- Career development within a globally recognized organization
