R&D Scientist I
Job
KCM Technical
Maple Grove, MN (In Person)
$68,640 Salary, Full-Time
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Job Description
R D Scientist I Maple Grove, MN 55369 $28
- $38 an hour
- Full-time, Contract $28
- $38 an hour
- Full-time, Contract Onsite
- Arbor Lakes Job Purpose The Scientist I has engineering/science education, basic technical skill set, and the ability to work in a team setting.
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 log books, 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 BSC Quality Policy. Establishes and promotes a work environment that supports the Quality Policy and Quality System. Education/Experience/Skills 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.Pay:
$28.00- $38.
Benefits:
401(k) Dental insurance Health insurance Paid time off Referral program Vision insuranceWork Location:
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