Biomedical Scientist I: Lab Research & Data Analysis

TALENT Software Services; Maple Grove (MN); On-site; USD 65,000 - 90,000; Full time

Job summary

TALENT Software Services is seeking a Scientist I in Maple Grove, MN. The role involves applying engineering and scientific skills to execute experiments and data analysis in support of medical device projects. It requires a BA/BS in Biology, Chemistry, or related field and at least two years of medical device experience.

You will work onsite, collaborate with a team, and contribute to method development, data documentation, and quality processes, while adhering to EH&S guidelines.

Qualifications

• BA/BS degree in Biology or Chemistry (or a related Engineering field).
• 2+ years of medical device experience.
• Hands-on approach to method development and data analysis.
• Ability to communicate complex ideas clearly, both orally and in writing.
• Experience managing multiple projects in a timeline-driven environment.
• Proficient computer skills: Word, Excel, PowerPoint, Adobe Acrobat.

Responsibilities

• Remain knowledgeable of technologies and literature within the functional area.
• Support testing of new technologies and targets for research.
• Generate data for posters, presentations, and internal documents.
• Develop understanding of experiments and SOPs; execute routine work independently.
• Apply basic data analysis and identify basic issues with data; compare with historical data.
• Summarize results and contribute to technical reports.

Skills

Self-motivation

Hands-on

Communication

Team player

Time management

Problem solving

Education

BA/BS Biology or Chemistry or related Engineering field

Tools

MS Word

Excel

PowerPoint

Adobe Acrobat

Minitab

Job description

TALENT Software Services is seeking a Scientist I in Maple Grove, MN. The role involves applying engineering and scientific skills to execute experiments and data analysis in support of medical device projects. It requires a BA/BS in Biology, Chemistry, or related field and at least two years of medical device experience.

You will work onsite, collaborate with a team, and contribute to method development, data documentation, and quality processes, while adhering to EH&S guidelines.