Scientist I # 26-25954

Us Tech Solutions; Maple Grove (MN); On-site; USD 65,000 - 90,000; Full time

Job summary

Us Tech Solutions seeks a Scientist I for a 12‑month contract to perform routine experiments, analyze data, and help prepare technical reports and presentations. You will work under direction with senior staff to develop methods, maintain notebooks, and ensure quality and EH&S compliance.

The role emphasizes hands-on method development, teamwork, and timely execution of multiple projects in a medical device context. Strong writing and communication skills are essential.

Qualifications

• BA/BS in Biology or Chemistry (or related Engineering field) required.
• 2+ years of medical device experience preferred.
• Strong problem-solving and data-analysis skills.
• Ability to document methods and results clearly in reports.

Responsibilities

• Perform routine experimental techniques and data analysis.
• Generate data to support posters, presentations, and internal documents.
• Prepare lab notebooks and technical reports with documentation.
• Assist with IQ/OQ activities and equipment maintenance as needed.
• Contribute to lab/infrastructure improvement projects.
• Ensure EH&S compliance and quality system adherence.

Skills

Self-motivation

Clear communication

Team player

Problem solving

Multi-project management

Computer skills

Documentation

Education

BA/BS in Biology or Chemistry (or related Engineering field)

Tools

Minitab

Design-Expert

DOE methodologies

Microsoft Office

Adobe Acrobat

Job description

Duration: 12 Months Contract (Extension Possible)

Job Purpose

• 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. Gaining knowledge in scientific/engineering concepts, business practices, and core business principles.

Job Duties:

• 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. DOE) 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 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 logbooks, materials receiving, and inventory control.
• Completes time records and reports projects allocated time.
• May participate in implementing solutions for lab/infrastructure improvement.

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.
• For those individuals that supervise others, the following statements are applicable:
• 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.

Education/Experience/Skills a candidate must have to successfully perform the above duties/tasks.

• 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
• Ability to communicate complex ideas clearly and simply, both orally and in writing
• 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 the software applications 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.

US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

AI Statement:

By applying, you acknowledge that AI-assisted tools may be used during hiring.