Medical Device Scientist I

Pay Range: $32.37hr - $41.33hr Job Overview: The Scientist I has engineering/science education, basic technical skill set, and the ability to work in a team setting. Applies engineering/scientific skills and commitment to quality to execute experiments and complete data analysis in support of projects. The successful candidate is gaining knowledge in scientific/engineering concepts, business practices, and core business principles. Job Duties: The candidate may participate in implementing solutions for lab/infrastructure improvement. Remains knowledgeable of technologies (including relevant literature) within functional area. Supports testing of new technologies and targets for research within functional area. Generates data to support posters, presentations, and internal documents. Utilizes knowledge of legal boundaries surrounding information sharing and documenting; may contribute to brainstorming for intellectual property. Develops an understanding of experiments/protocols (e.g. Design of Experiments) and design process; executes under direction; completes routine work independently within functional area. Applies basic data analysis; develops understanding of more complex data analysis; identifies basic problematic issues with data; compares results with historical data. Summarizes results, contributes to the generation of technical reports, and completes experimental paperwork/lab notebook documentation. Develops methods and processes under direction from senior technical staff. Participates as an extended team member for experimental execution. Performs assigned routine experimental techniques and processes according to functional area. Orders supplies and may submit sample requests as directed by more senior staff and per the standard operating procedure (SOP). May perform equipment maintenance and generate and execute equipment IQ/OQ as needed. Adheres to all EH&S procedures and general housekeeping SOPs. Complies with site and department specific procedures on record keeping, use of log books, materials receiving, and inventory control. Completes time records and reports project-allocated time. Quality System Requirements: In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the Quality Policy. Establishes and promotes a work environment that supports the Quality Policy and Quality System. Requirements: BA/BS degree in Biology or Chemistry (or a related Engineering field). 2+ years of medical device experience. Self-motivation with a passion for solving problems. Hands-on approach to method development. Strong verbal and written communication skills. Demonstrated ability to effectively manage multiple projects and priorities in a timeline-driven environment. Team player with excellent interpersonal skills. Computer skills, including experience with software applications such as Microsoft Word, Excel, PowerPoint, and Adobe Acrobat. Prior experience in test documentation through lab notebooks or reports. Preferred Qualifications: Test Method development experience. Knowledge of Minitab. Competent in Design of Experiments methodology (i.e. Design-Expert), scientific method, and statistical analysis software (i.e. Minitab). Strong problem-solving skills. Demonstrated experience analyzing and fulfilling documentation requirements. Experience in medical device industry, preferably testing medical devices. Benefits: Our Benefits Include: Medical, Dental, and Vision Insurance 401(k) Retirement Plan Health Savings Account (HSA) Disability Insurance (Short-Term and Long-Term) Life and AD&D Insurance Paid Sick Leave (where required by applicable state or local law) Supplemental Insurance Plans Identity Theft Protection Pet Insurance Employee Wellness Programs Employee Assistance Program (EAP) Career Growth and Professional Development Opportunities Disclaimer: Benefits eligibility, accrual rates, and usage limits may vary based on employment status, length of service, and work location. Paid Sick Leave is provided in strict accordance with applicable state and municipal mandates. Cynet Systems Inc. reserves the right to modify, amend, or terminate any benefit plans at any time in accordance with applicable laws. About Cynet Systems Founded in 2010 and headquartered in the Washington, DC metro area, Cynet Systems Inc. is a leading technology staffing and workforce solutions company serving Fortune 500 companies, government agencies, and enterprise organizations across the United States and Canada. We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and professional staffing, powered by a high-performing recruitment engine operating across North America and Asia. As a nationally and locally certified Minority Business Enterprise (MBE), Cynet Systems is committed to helping organizations build high-performing teams while empowering professionals to grow rewarding careers. Our organization is certified to ISO 9001, ISO 14001, ISO 27001, and SOC 2 Type II standards, reflecting our commitment to quality, security, operational excellence, and customer success.