Intern- Regulatory Affairs
On-siteCentral, Louisiana, United States
Job Summary
Prepare and submit product registration updates to secure approvals across the portfolio. Monitor, collect, and synthesize regulatory updates from official government portals and industry sources. Manage internal tracking databases to maintain high data integrity and accuracy. Assist with automating manual processes using internal digital tools to optimize team efficiency. Collaborate with cross-functional partners on regulatory and quality projects. Support special Q&R tasks as needed. This 4 to 6-month internship provides a gateway to understanding Quality and Regulatory compliance within the medical device industry at Roche Diagnostics.
Required Qualifications
- Currently pursuing a Degree in Biomedical Science, Pharmacy, Biomedical Engineering, Life Sciences, or a related field
- Exceptionally meticulous with a high sense of responsibility and personal ownership over data accuracy, tracking databases, and regulatory compliance
- A fast learner who takes initiative, manages time effectively, and thrives when working independently with minimal supervision
- Highly comfortable with technology, with a natural ability to quickly adapt to new software, internal digital tools, and workflow automation systems
- Excellent verbal and written communication skills
- An enthusiastic, proactive attitude
- Able to commit for 4 to 6 months internship duration
- Exact available commitment dates clearly stated at the top of the resume
Desired Qualifications
- A genuine curiosity about medical device regulations and how they shape healthcare innovation
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