Latest Life Science Jobs at Beckman | Apply Now for Regulatory Affairs Intern
Are you a life sciences student eager to start your career in regulatory affairs? Beckman Coulter Life Sciences, a global leader in biotechnology and diagnostics, is offering an exciting internship opportunity in Miami, Florida. As a Regulatory Affairs Intern, you will gain hands-on experience in compliance, documentation, and regulatory strategy, working closely with cross-functional teams to accelerate solutions that improve human health.
About Beckman Coulter Life Sciences
At Beckman Coulter Life Sciences, part of Danaher Corporation, our work in life sciences, diagnostics, and biotechnology saves lives. We are committed to innovating for tangible impact and providing new solutions to transform human health. Join us in accelerating answers and making a real difference.
Job Details
- Job Post: Regulatory Affairs Intern
- Company: Beckman Coulter Life Sciences
- Location: Miami, Florida, United States of America
- Category: Intern
- Job ID: R1295247
Qualifications
- Currently pursuing a bachelor’s or master’s degree in Regulatory Affairs, Life Sciences, Pharmacy, Public Health, or related discipline
- Strong attention to detail, organizational skills, and excellent written and verbal communication abilities
- Familiarity with regulatory terminology and documentation practices
- Ability to work independently and in a team environment
Preferred qualifications include:
- 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)
Position Overview
The Regulatory Affairs Intern at Beckman Coulter Life Sciences will gain hands-on experience in regulatory strategy, documentation, and compliance within the life sciences industry. This role involves supporting regulatory submissions, ensuring alignment with global standards, and collaborating with cross-functional teams.
Key Responsibilities
- Assist in the preparation, review, and submission of regulatory documents to health authorities
- Support regulatory tracking systems and maintain documentation databases
- Research 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
Compensation
The hourly range for this role is $30.00.
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