Prime Path Medtech™ · 4 hours ago
Project Engineering Intern
Prime Path Medtech is seeking a Project Engineering Intern to support their Regulatory, Clinical, and Quality consulting teams. This part-time internship is designed for junior or senior undergraduate students interested in a career in the medical device industry, providing hands-on exposure to quality systems and regulatory documentation.
Artificial Intelligence (AI)Clinical TrialsTraining
Responsibilities
Support the development and maintenance of client quality management system (QMS) documentation, including SOPs, templates, and controlled documents aligned with regulatory standards
Assist with technical and regulatory writing, document organization, and formatting for medical device projects
Participate in internal and client project meetings to observe and support regulatory and quality activities
Help review and organize quality and regulatory documentation, such as:
SOPs and Work Instructions
Risk management files
Design and technical documentation
Clinical and regulatory support materials
Support clinical research and regulatory projects through data organization, document preparation, and coordination tasks
Assist with maintaining documentation within controlled document systems (version control, approvals, change tracking)
Learn and apply domestic and international medical device regulatory requirements through hands-on project work
Provide general project support to ensure work is delivered accurately, on time, and to Prime Path quality standards
Qualification
Required
Currently pursuing a Bachelor's degree in Engineering, Life Sciences, or a related field
Junior or Senior standing preferred
Strong written communication and organizational skills
Interest in medical devices, regulatory affairs, quality systems, or clinical research
Proficiency with Microsoft Office (Word, Excel, PowerPoint, Outlook) and Adobe Acrobat
Preferred
Previous internship, coursework, or experience in a medical, technical, or regulated environment
Experience or interest in technical or scientific writing
Familiarity with document management or version-controlled systems (academic or professional)
Ability to manage multiple tasks and meet deadlines
Self-motivated, detail-oriented, and eager to learn
Comfortable working both independently and as part of a team
Company
Prime Path Medtech™
We partner with companies at all stages to achieve business outcomes – from strategic regulatory planning to all phases of the product development process to get your product on the market.
Funding
Current Stage
Early StageRecent News
2024-11-24
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