R&D Technician II

Scientific Plymouth, Minnesota Contract Jul 27, 2026 Location: Plymouth, Minnesota Work Arrangement: Fully onsite Travel: Local travel to additional worksites in Minnetonka and St. Paul may be required Classification: Nonexempt; hours worked over 40 per week are eligible for overtime pay at 1.5 times the regular hourly rate Position Overview Viltis is seeking an R&D Technician II on behalf of our client to support laboratory testing, product development, and characterization activities for innovative medical technologies. This hands‑on position will work closely with technicians, engineers, and scientists to execute experimental studies and generate accurate, reliable, and well‑documented scientific data. The technician will perform laboratory testing, prepare samples, operate test equipment, collect and analyze data, and maintain documentation in accordance with established procedures and quality requirements. The ideal candidate is detail‑oriented, scientifically curious, dependable, and motivated by hands‑on laboratory work. This individual should be comfortable following established protocols, learning new experimental methods, and working both independently and collaboratively in a regulated laboratory environment. Key Responsibilities Perform hands‑on laboratory testing and experimental studies in support of research and product development activities. Support in vitro preclinical testing, device characterization, verification testing, and process development. Prepare test samples, materials, laboratory equipment, and experimental setups. Execute test protocols, study plans, written procedures, and standard operating procedures. Operate, maintain, and assist with troubleshooting laboratory and test equipment. Collect, organize, and document experimental data with a high degree of accuracy, precision, and repeatability. Review and analyze test results to identify trends, observations, anomalies, and potential issues. Prepare technical reports, study documentation, protocols, summaries, and other project records. Maintain accurate laboratory records in accordance with established quality and documentation requirements. Support the development and improvement of laboratory methods and testing processes. Maintain laboratory organization, cleanliness, inventory, and equipment readiness. Communicate experimental findings and project updates to engineers, scientists, technicians, and other cross-functional team members. Travel locally to worksites in Plymouth, Minnetonka, and St. Paul as needed. Contribute to a positive, collaborative, and productive laboratory environment. Required Qualifications One to four years of experience in a laboratory, R&D, product testing, medical device, biotechnology, manufacturing, or related technical environment; or a bachelor’s degree in a relevant field. Hands‑on experience performing laboratory testing or executing experimental procedures. Experience collecting, documenting, and organizing experimental data. Ability to operate laboratory or test equipment and follow established procedures, protocols, and SOPs. Strong attention to detail and commitment to producing accurate, reproducible, and well‑documented results. Strong analytical and critical‑thinking skills. Proficiency with Microsoft Excel and basic data analysis. Strong written communication, documentation, and organizational skills. Ability to learn new laboratory techniques, methods, equipment, and technologies quickly. Ability to work independently on routine assignments while also collaborating effectively within a team. Ability to work fully onsite and travel locally between designated Minnesota worksites. Preferred Qualifications Associate’s or bachelor’s degree, technical certification, or equivalent hands‑on experience in Engineering, Biomedical Sciences, Biology, Chemistry, or a related technical field. Experience supporting in vitro or preclinical laboratory testing. Experience working in a regulated laboratory, medical device, biotechnology, or quality‑controlled environment. Experience with device characterization, verification testing, or product development activities. Experience analyzing experimental data and preparing technical reports, study plans, protocols, or other controlled documentation. Experience troubleshooting laboratory or test equipment. Ideal Candidate The successful candidate will be proactive, dependable, organized, and easy to work with. They will demonstrate scientific curiosity, sound judgment, and a team‑oriented approach while consistently producing high‑quality work. This individual should be comfortable managing routine assignments independently, communicating potential issues promptly, and partnering closely with technical team members to achieve project objectives. About Viltis Viltis is a life sciences consulting and talent solutions firm supporting pharmaceutical, biotechnology, and medical technology organizations. We connect experienced professionals with opportunities where they can contribute to meaningful scientific, engineering, quality, clinical, and regulatory initiatives. Viltis is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, sex, national origin, age, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by applicable law. #J-18808-Ljbffr Viltis