Scientist I – Medical Device Testing & Method Development

Location: Maple Grove, MN 55369

Job Type: Year Long Contract with opportunity to extend

Pay Rate: $39.00 an hour or about $79,000 a year

Work Authorization: Applicants must be authorized to work in the U.S. without current or future visa sponsorship. Sponsorship is not available for this role.

Position Overview

We are seeking a motivated Scientist I to support testing, method development, and experimental execution within a medical device research and development environment. This role is ideal for an early-career scientist or engineer with hands-on laboratory experience, strong documentation skills, and the ability to work collaboratively in a fast-paced, timeline-driven setting.

The Scientist I will apply scientific and engineering principles to conduct experiments, analyze data, support technical documentation, and contribute to research initiatives. The ideal candidate will have prior medical device industry experience and a passion for problem-solving and laboratory-based development work.

Key Responsibilities

Execute laboratory experiments, testing activities, and routine experimental techniques within the functional area
Support development and evaluation of new technologies, methods, and research targets
Perform data analysis and compare results against historical trends and expectations
Generate technical documentation including lab notebooks, reports, presentations, and supporting materials
Contribute to technical reports, posters, and internal project documentation
Assist with test method development and experimental protocol execution under guidance from senior staff
Apply basic statistical analysis and identify data inconsistencies or issues
Maintain accurate documentation in compliance with SOPs and quality requirements
Participate in cross-functional project teams to support experimental execution and project timelines
Order laboratory supplies and coordinate sample requests as needed
Perform equipment maintenance activities and assist with IQ/OQ documentation when required
Ensure compliance with EH&S procedures, quality standards, housekeeping requirements, and inventory control processes
Remain current on relevant scientific literature and technologies within the functional area

Quality & Compliance Responsibilities

Demonstrate a strong commitment to patient safety and product quality
Maintain compliance with all quality systems, procedures, and documentation requirements
Follow site-specific procedures related to record keeping, materials handling, and laboratory operations
Accurately complete time tracking and project allocation reporting

Required Qualifications

Bachelor’s degree in Biology, Chemistry, Engineering, or a related scientific field
2+ years of experience within the medical device industry
Hands-on laboratory experience with testing and/or method development
Strong problem-solving and analytical skills
Ability to manage multiple priorities in a fast-paced, timeline-driven environment
Strong written and verbal communication skills
Experience with laboratory documentation, lab notebooks, and technical reports
Proficiency with Microsoft Office applications including Word, Excel, PowerPoint, and Adobe Acrobat
Self-motivated team player with strong interpersonal skills

Preferred Qualifications

Test method development experience
Experience testing medical devices
Knowledge of Minitab and statistical analysis software
Familiarity with Design of Experiments (DOE) methodologies and tools such as Design-Expert
Experience supporting documentation and compliance requirements in regulated environments
Strong scientific data analysis capabilities

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