Internship Session Summer 2025 Term/duration College Level/New Grad 10 weeks Start Date June 9, 2025 End Date August 15, 2025 Title Regulatory Affairs & Quality Assurance Intern Department Regulatory Affairs and Quality Assurance Reporting Line SVP, Regulatory Affairs & Quality Assurance Location 1. On-site Program Scottsdale, Arizona - Headquarters Application Apply via online application posting Education College Level/New Grad: Must be an actively enrolled and in good standing with their program Condition Paid internship Internship for school credit Both (evaluated on a per applicant basis) Compensation Minimum wage of the applicable work state Benefits If during an internship, work-related travel is necessary: CND reimbursed travel expenses Per diem meal stipend Required Training Upon their start date, all interns will be required to complete the following training: New Hire Security Training Semi-Annual Cyber Training Any interns with access to patient health information will also be required to complete the following training: Steri-Safe: Annual HIPAA Staff Training Steri-Safe: Advanced HIPA Any interns with a lab component of their internship will be required to complete the following trainings: DOT Training Steri-Safe: BBP Training Biohazardous Waster Training Steri-Safe: Hazardous Communication Training Process Online application submitted followed by an interview. CND background check to include drug screen for all accepted applicants. Completion of CND onboarding documents Overview We are seeking a motivated and detail-oriented intern to join our Quality and Regulatory team. This internship provides a valuable opportunity to gain hands-on experience in quality assurance and regulatory affairs within the medical device sector. The intern will support a variety of projects aimed at ensuring compliance with applicable industry standards and regulatory requirements. Key Responsibilities: Assist in drafting, reviewing and updating quality assurance documentation such as standard operating procedures (SOPs), work instructions, and quality manuals. Support the preparation of regulatory submissions and ensure compliance with domestic and international regulations (e.g., FDA, ISO, EU MDR). Participate in internal audits and inspections to help ensure alignment with quality standards. Assist in organizing maintaining regulatory records and documentation. Conduct research on relevant regulations and best practices in quality compliance. Collaborate with cross-functional teams to support resolution of quality and regulatory issues. Contribute to investigations and corrective actions related to non-conformances. Support implementation of quality improvement initiatives and electronic quality management systems (eQMS). Qualifications: Currently pursuing a Master's degree in Engineering, Life Sciences, Regulatory Affairs, or a related field. Strong interest in quality assurance and regulatory compliance. Excellent organizational skills with the ability to manage multiple tasks and deadlines. Strong analytical thinking and problem-solving abilities. Clear and effective communication and interpersonal skills. Ability to work both independently and collaboratively. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). CND Life Sciences
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