This is an exciting new opportunity for a Quality Intern at Click Therapeutics:
About Click Therapeutics
Click Therapeutics, Inc. develops, validates, and commercializes software-based prescription medical treatments designed for individuals with unmet medical needs. As a leader in Digital Therapeutics™, Click provides clinically validated, FDA-regulated prescription treatments that are accessible via smartphones. With a commitment to scientific rigor, patient-centric design, and advanced technology, Click creates engaging therapeutic experiences that deliver meaningful clinical outcomes.
Click continuously enhances its platform through innovative cognitive, behavioral, and neuromodulatory mechanisms, incorporating cutting-edge AI and machine learning tools. The company’s digital therapeutics pipeline spans multiple therapeutic areas, including psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently recognized as a top workplace, Click fosters an inclusive and diverse team of innovators, clinicians, scientists, researchers, designers, and engineers, all working toward the shared goal of expanding access to safe and effective prescription digital therapeutics. More details can be found at www.clicktherapeutics.com and on LinkedIn.
About The Role
Click Therapeutics is seeking an ambitious and detail-oriented Quality Intern to join its Quality Team and contribute to the development of Software as a Medical Device (SaMD) products. This role offers a unique opportunity to gain hands-on experience in the growing digital health sector while learning about medical device quality system principles, Agile software development, and cross-functional collaboration to support quality system processes.
This hybrid internship is based at Click’s headquarters in Tribeca, NYC, placing the intern at the heart of a rapidly expanding digital health community. Interns are expected to be in the office on Wednesdays and Fridays.
Responsibilities
Assist in the implementation and oversight of Click’s Quality Management System (QMS) processes across the organization.
Support product development activities, including risk management and design reviews, ensuring compliance with regulatory and quality standards throughout the Software Development Lifecycle.
Manage records within Click’s electronic QMS document management system, including CAPA records, complaints, and training documentation.
Review design documentation such as product requirements, design specifications, and verification/validation test plans and reports, maintaining records within the Design History File (DHF).
Contribute to the enhancement of quality system procedures to facilitate continuous process improvements and the expansion of Click’s quality system for product commercialization in global markets.
Conduct research on SaMD and Digital Therapeutics (DTx) industry trends, FDA updates, and international standards, applying key insights to Click’s Quality Management System.
Qualifications
Rising sophomore or junior currently pursuing an undergraduate degree.
Strong verbal and written communication skills.
Excellent attention to detail and organizational abilities.
Passion for digital health and healthcare innovation.
Preferred Qualifications
Pursuing a degree in Biomedical Engineering, Biological Engineering, or a related field.
Experience with technical writing, including SOPs, in a scientific or engineering context.
Familiarity with software programming languages.
Basic knowledge of medical device regulations and standards such as FDA 21 CFR Part 820, ISO 13485, ISO 14971, and IEC 62304.
Compensation
$22 per hour.
Hours And Duration
Part-time, 30 hours per week.
Internship duration: 10 weeks, from May 20th to August 1st, 2025.
Benefits
Mac laptop provided
Sponsored company events
Unlimited office snacks and beverages
Additional perks
Equal Employment Opportunity
Click Therapeutics is dedicated to providing equal employment opportunities to all employees and job applicants, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, age, national origin, disability, or veteran status. The company complies with all applicable national, state, and local employment laws, including employment eligibility verification requirements. Applicants must have authorization to work in the U.S. Click Therapeutics may, at its discretion, support visa applications or sponsorship based on factors such as availability of qualified U.S. workers and long-term employment prospects.
Employment sponsorship inquiries should be disclosed at the time of application. Any sponsorship or visa support provided by Click Therapeutics does not alter the at-will employment relationship between the company and the employee.
