About Discovery Life Sciences:
Discovery Life Sciences (Discovery) is a leading provider of highly characterized human biospecimens and cellular starting materials to advance cell and gene therapy and precision medicine programs for cancer, infectious disease, and other complex conditions. We routinely manage hundreds of studies and expertly test thousands of biospecimens simultaneously. Leading biopharma, diagnostic and academic institutions trust us to quickly deliver high-quality biospecimens and reliable, reproducible biomarker data, so they can outpace their competition and push the leading edge of innovation using our Science at your Service TM business model.
Position Summary:
Discovery is seeking motivated interns to join our Regulatory team for the upcoming spring and summer semesters. This role will provide hands-on experience in regulatory compliance and quality systems within the organization. The Intern will assist in gap assessments, regulatory research, and documentation to support compliance with international standards and local regulations.
Must-Have Qualifications (Education, Skills, Experience):
- Currently enrolled in a Bachelor’s or Master’s program in life sciences preferred or other related fields such as legal may be considered
- Interest in regulatory compliance and quality systems in the biotechnology industry
- Strong attention to detail and organizational skills
- Ability to conduct research and interpret complex concepts
- Proficient in Microsoft Office Suite (Excel, Word, PowerPoint). Some prior experience with Smartsheet would be beneficial
- Excellent written and verbal communication skills
Key Responsibilities:
Regulatory Gap Assessments:
- Perform gap analyses for applicable regulatory requirements, ISO standards, and guidelines
- Identify areas for improvement and document findings
Management Review Support:
- Assist in evaluating changes to regulatory requirements impacting the Tissue Biomarker Services sites (US and EU)
- Prepare summaries and reports for management review meetings related to regulatory requirements
Database Development:
- Compile a list of applicable local regulations for each site
- Create and maintain a comprehensive database of regulatory requirements for:
- GCLP (Good Clinical Laboratory Practice)
- ISO 17020
- Other relevant standards and guidelines
IRB Reporting Support:
- Assist in preparing Institutional Review Board (IRB) annual reports and related documents
Compensation and Benefits:
- This is a “for credit” internship. The selected candidate will not be entitled to compensation, benefits, or paid time off.
Location and work hours:
- Onsite Huntsville, AL
- Part-time – 6 to 20 hours per week during the Spring or Summer 2026 semester
- Applications for this position will be accepted until the role has been filled.
We are actively seeking motivated, dedicated individuals like you to join our thriving organization. As a leader in our industry, we offer unparalleled opportunities for professional growth and success.
The Discovery Life Sciences Talent Acquisition team proudly manages and represents all Discovery recruitment activities. We respectfully request that third party staffing agencies refrain from submitting candidates or soliciting meetings to discuss recruiting services.
We are unable to sponsor or take over sponsorships of any applicant work visas at this time.
Apply Now to join our team!
Visit dls.com/careers for more details.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
Top Skills
What We Do
Discovery Life Sciences, the Biospecimen and Biomarker Specialists™, is a leading provider of highly characterized human biospecimens and cellular starting materials integrated with expert multi-omic analytical services to advance cell and gene therapy and precision medicine programs for cancer, infectious disease, and other complex conditions. Our robust biospecimen and biomarker platform is optimized for speed and large scale capacity. We routinely manage hundreds of studies and expertly test thousands of biospecimens simultaneously as a single vendor - eliminating time consuming and inefficient transfers of biospecimens or data between different vendors. We offer one of the largest recallable donor pools, Research Use Only (RUO) and clinical-grade (GMP) fresh and cryopreserved human cellular materials to support cell and gene therapy programs at any scale from start to finish. Leading biopharma, diagnostic and academic institutions trust us to quickly deliver high-quality biospecimens and reliable, reproducible biomarker data, so they can outpace their competition and push the leading edge of innovation. Visit www.dls.com to learn more









