Job Posting: Scientist I Location: Maple Grove, MN Pay Rate: $40.00–$41.33 per hour Schedule: Monday–Friday, 8:00 AM–4:30 PM Desired Start Date: October 26, 2026 Assignment Duration: 12 months Position Type: Contract Work Arrangement: Onsite Position Overview We are seeking a motivated and detail-oriented Scientist I to support research, testing, and development activities within a medical device environment. This role is ideal for a science or engineering professional with hands-on laboratory experience, strong analytical skills, and an interest in test method development and product quality. The Scientist I will execute experiments, analyze data, document results, and collaborate with cross-functional teams to support research projects and new technology development. The successful candidate will demonstrate a commitment to scientific accuracy, problem-solving, regulatory compliance, and patient safety. Work Authorization Requirement: Candidates must be authorized to work in the United States without visa sponsorship now or in the future. Applicants who require current or future sponsorship cannot be considered.
Key Responsibilities
- Execute laboratory experiments, testing procedures, and routine technical processes to support research and development projects.
- Support the evaluation and testing of new technologies and research targets.
- Follow experimental protocols, including Design of Experiments (DoE), under the direction of senior technical staff.
- Perform data analysis, identify potential data issues, and compare results against historical findings.
- Summarize experimental results and contribute to technical reports, presentations, posters, and internal documentation.
- Maintain accurate laboratory notebooks, experimental records, and technical documentation.
- Assist with the development and improvement of testing methods and laboratory processes.
- Stay current with relevant scientific technologies, testing methods, and technical literature.
- Collaborate with cross-functional teams to execute experiments and meet project deadlines.
- Order laboratory supplies, submit sample requests, and support inventory control according to established procedures.
- Perform equipment maintenance and assist with Installation Qualification and Operational Qualification (IQ/OQ), as needed.
- Follow Environmental, Health, and Safety (EH&S) requirements and laboratory housekeeping procedures.
- Comply with site and departmental procedures for recordkeeping, logbooks, materials receiving, and inventory management.
- Complete time records and track project hours accurately.
- Contribute to laboratory and infrastructure improvement initiatives.
- Maintain compliance with quality policies and procedures, prioritizing patient safety and product quality.
Required Qualifications
- Bachelor's degree in Biology, Chemistry, a related scientific discipline, or an engineering field.
- At least two years of experience in the medical device industry.
- Hands-on experience with laboratory testing, experimental procedures, or technical method development.
- Strong problem-solving skills and a self-motivated approach to scientific work.
- Ability to communicate complex technical concepts clearly, both verbally and in writing.
- Ability to manage multiple projects and priorities in a deadline-driven environment.
- Strong interpersonal skills and the ability to work effectively within a team.
- Experience documenting laboratory testing through notebooks, reports, or other technical records.
- Proficiency in Microsoft Word, Excel, PowerPoint, and Adobe Acrobat.
- Authorization to work in the United States without current or future visa sponsorship.
Preferred Qualifications
- Experience developing test methods.
- Experience testing medical devices, preferably in the medical device industry.
- Familiarity with Minitab or other statistical analysis software.
- Knowledge of Design of Experiments (DoE) methodology, including tools such as Design-Expert.
- Understanding of the scientific method, experimental design, and statistical analysis.
- Strong analytical thinking and troubleshooting abilities.
- Experience reviewing and fulfilling technical documentation requirements.
- Familiarity with quality systems, laboratory procedures, and product quality standards.
Schedule and Assignment Details
- Location: Maple Grove, Minnesota
- Work Arrangement: Onsite
- Shift: First shift, 8:00 AM–4:30 PM
- Start Date: October 26, 2026
- Contract Length: 12 months
- Hourly Pay: $40.00–$41.33
Benefits and Paid Leave Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an Employee Assistance Program (EAP), commuter benefits, DailyPay, and a 401(k) plan. Our benefits program provides employees with the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include paid sick leave where required by law, any other paid leave required by federal, state, or local law, and holiday pay upon meeting applicable eligibility criteria. How to Apply Qualified candidates with a background in science or engineering, medical device experience, and strong laboratory testing and documentation skills are encouraged to apply.
Pay Details: $40.00 to $41.33 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
Military connected talent encouraged to apply
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