Internships

Employer: Northeast Biomedical Expires: 07/23/2026 About Northeast BiomedicalNortheast Biomedical (NEB) is an ISO 13485-certified medical device product development and contract manufacturing company specializing in helping innovators transform ideas into commercially successful medical devices. Our multidisciplinary team partners with startups, physicians, entrepreneurs, and established medical device companies to develop technologies from concept through commercialization.Our work spans a broad range of medical technologies, including cardiovascular devices, surgical instruments, implants, drug delivery systems, diagnostics, and other innovative healthcare products. We combine engineering expertise, quality systems, regulatory knowledge, and manufacturing capabilities to accelerate product development and reduce risk for our clients.Position SummaryNEB is seeking a Design Quality Engineer to support the development of innovative medical devices within a fast-paced consulting and product development environment. This position reports directly to Phil Andrusin, Vice President of Engineering, and works closely with engineering, manufacturing, quality, and project teams throughout the product development lifecycle.The Design Quality Engineer will be responsible for ensuring that quality and regulatory requirements are effectively integrated into product development activities from concept through commercialization. This role includes participation in design controls, risk management, verification and validation, product transfer, and quality system improvement initiatives.Candidates with a wide range of experience are encouraged to apply. The final level, responsibilities, and compensation will be determined based on qualifications, technical expertise, and relevant industry experience.ResponsibilitiesSupport and lead design control activities throughout product development programs.Develop and maintain Design History Files (DHFs) and supporting quality documentation.Participate in product requirements development, traceability, and design review activities.Lead or support risk management activities, including hazard analyses, FMEAs, and risk-benefit assessments.Collaborate with engineering teams to ensure compliance with applicable regulatory and quality requirements.Develop, review, and approve protocols and reports for verification and validation activities.Support design verification, design validation, and process validation efforts.Review engineering documentation, specifications, drawings, and test reports for quality compliance.Participate in change control activities and engineering change assessments.Investigate nonconformances and support root cause analysis and corrective action activities.Support manufacturing transfer and production readiness activities.Participate in internal and external audits.Contribute to continuous improvement initiatives within NEB's ISO 13485-certified Quality Management System.Interface directly with clients on project-specific quality and regulatory matters as required.Support compliance with FDA regulations, ISO standards, and customer requirements.QualificationsRequiredBachelor's degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemical Engineering, Quality Engineering, or a related technical discipline.0-10 years of experience in medical device, biotechnology, pharmaceutical, or other regulated industries.Strong technical writing and documentation skills.Excellent organizational and project management abilities.Strong analytical and problem-solving skills.Effective verbal and written communication skills.Ability to work independently and collaboratively within multidisciplinary teams.Proficiency with Microsoft Office applications.PreferredExperience with medical device design controls.Familiarity with ISO 13485 and FDA Quality System requirements.Experience developing and maintaining Design History Files.Experience with risk management methodologies, including FMEA.Experience supporting verification and validation activities.Familiarity with statistical analysis and quality engineering tools.Experience supporting audits, CAPA activities, and quality system improvements.Familiarity with IEC, ISO, FDA, and other applicable medical device standards and regulations.Position LevelNEB is seeking candidates across a broad range of experience levels. Individuals early in their careers who are eager to learn and experienced quality professionals looking for greater technical responsibility are both encouraged to apply.The final title, responsibilities, and compensation package will be commensurate with experience, demonstrated technical capability, and industry expertise.Why Join NEB?Work on a diverse portfolio of innovative medical device technologies.Gain exposure to the entire product development lifecycle.Collaborate with experienced engineers, scientists, and manufacturing professionals.Work directly with company leadership and technical experts.Contribute to products that improve patient outcomes and quality of life.Join a growing organization with opportunities for professional advancement and leadership development.BenefitsNEB offers a competitive compensation and benefits package, including health insurance, paid time off, retirement savings opportunities, professional development support, and participation in a collaborative, innovation-focused work environment.Northeast Biomedical is an Equal Opportunity Employer and values diversity in the workplace.

Employer: Sustainable Energy Advantage, LLC Expires: 07/27/2026 It’s time. Technology, economic, policy and climate drivers are converging to drive a rapidly expanding renewable energy landscape, and Sustainable Energy Advantage (SEA) is right in the middle of it. In our realm, new opportunities are popping up almost daily. Our widely respected and growing renewable energy consulting / advisory firm provides our exceptionally broad and varied client base with expertise, analysis, insights, and tools to succeed. If you crave variety, possess a well-rounded skill set, analytical mind, and want to do something you can be passionate about, keep reading. Join a tight-knit and motivated team of about 20 professionals in a collegial environment that thrives on passion with a shared sense of purpose (and humor). Be widely respected and never bored.  OPPORTUNITY:   We are seeking an enthusiastic, dedicated, and organized Research Associate intern capable of contributing to a thriving consulting practice in supporting the needs of a diverse set of clients and tasks. In this position, you will perform research as well as quantitative market, financial, and economic analysis pertaining to the renewable energy industry. This position represents an opportunity to gain exposure to, and experience with, a wide range of topics and stakeholders active in the renewable energy industry. As an SEA intern, you won’t be stuck with the same typical intern drudgery, day after day. You’ll participate in (or even host!) Brown Bag Breakfasts, our own version of Lunch & Learns; you’ll work on a wide variety of projects and tasks, together with Senior staff; and your work will get into the hands of our subscribers and clients. At SEA, we take time to make sure you are comfortable but also given space to breathe, understand, and adapt. You’ll have a Mentor and a Supervisor, Senior staff that is invested in you and your career - even if you’re only with us for a short while. And you never know – you might just like us enough you’ll want to stay, something that one-third of our current staff have done!RESPONSIBILITIES:    Above all, the qualified candidate will be motivated and able to undertake a range of responsibilities that may include, but will not be limited to:Monitoring and summarizing current renewable energy regulatory, legislative and policy developments;Performing detailed research and analysis (qualitative and quantitative) on various renewable energy-related policy and business activities, including supply and demand within New England’s REC markets at present and using future projections;Supporting the development of new SEA products and services.Click here for some of what our prior interns have said about working at SEA, and click here for a full job description.

Employer: Southern Illinois University School of Medicine - SIU Medicine Expires: 07/29/2026 Are you interested in studying cancer, microbiology, immunology, or brain function recovery after an injury? Are you passionate about cutting-edge research in neurological disorders, neuroscience, developmental biology, cellular processes, molecular mechanisms, reproductive biology, and endocrinology? What about researching decision-making, skeletal muscle physiology, sensory processing, stem cell function, age-related diseases, or the impact of stress on aggression?Consider furthering your education at Southern Illinois University School of Medicine's Multidisciplinary Biomedical & Biological Sciences Graduate Program for the following Concentrations:• Anatomy & Neurobiology• Biochemistry and Molecular Biology• Microbiology• Molecular and Integrative PhysiologyThe MBBS Graduate Program offers financial assistance to graduate students through assistantships that include a stipend and a tuition waiver. Students may be offered either a Research Assistantship or a Teaching Assistantship.Research assistants perform data analysis and basic science experiments relevant to their mentor’s research area, such as cell culture, PCR, immunostaining, electrophysiology, etc.  In addition to developing their own project for their thesis or dissertation, they are expected to produce data for their mentor’s grants and publications. Research assistants are also expected to assist with general lab duties such as making buffers, taking care of the animal colony, and cleaning/autoclaving supplies. However, the specifics of each role will vary depending on the lab.Teaching assistants teach a laboratory section of an undergraduate physiology or microbiology course each semester, prepare an introductory talk for the undergraduate laboratory section, and grade lab reports and other assignments as appropriate for the course. They are expected to have office hours to meet with undergraduate students in their laboratory section. The specifics of each role will vary depending on the Concentration.Click here to apply today! https://www.siumed.edu/mbbs/mbbs-graduate-program-application-and-admissions