Scientist I

Actalent; Maple Grove (MN); On-site; USD 43,000 - 50,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) retirement plan

Life Insurance

Short and long-term disability

HSA

Job summary

Actalent seeks a Scientist I for an onsite laboratory role in Maple Grove, MN. The position focuses on designing and executing experiments, analyzing data, and supporting R&D within the medical device field to ensure product quality and patient safety.

You will generate reliable data, develop methods, and document results according to quality systems and SOPs. The role emphasizes adherence to quality processes, safety standards, and collaboration with R&D and QA teams.

Qualifications

• Bachelor's degree in Biology, Chemistry, or a related Engineering field.
• At least 2 years of experience in the medical device industry.

Responsibilities

• Stay current on technologies, scientific advancements, and relevant literature to inform experimental design and method development.
• Generate high-quality data to support internal documents, technical posters, and presentations.
• Perform assigned routine experimental techniques and laboratory processes in accordance with SOPs.
• Assist in IQ and OQ protocols and equipment maintenance.
• Adhere to EH&S procedures and maintain proper documentation and record keeping.

Skills

DOE understanding

Data analysis

Experiment design

Technical reporting

Literature review

Education

BA/BS in Biology, Chemistry, or related Engineering field

2+ years medical device experience

Job description

Scientist I

Major Device Company

Offers Benefits

Long-Term Growth

Job Description

The Scientist I role is an onsite, laboratory-based position that applies engineering and scientific knowledge to design and execute experiments, analyze data, and support research and development activities within the medical device field. This position contributes directly to product quality and patient safety by generating reliable data, supporting test method development, and maintaining accurate documentation in accordance with established quality systems and standard operating procedures.

Responsibilities

• Remain current on technologies, scientific advancements, and relevant literature within the functional area to inform experimental design and method development.
• Support the evaluation and testing of new technologies and research targets within the laboratory and broader functional area.
• Generate high-quality data to support internal documents, technical posters, and presentations.
• Utilize an understanding of legal boundaries surrounding information sharing and documentation, and contribute to brainstorming activities related to intellectual property under guidance.
• Develop an understanding of experimental protocols and design processes, such as Design of Experiments (DOE), and execute experiments under direction while performing routine work independently.
• Apply basic data analysis techniques, build proficiency in more complex data analysis, identify issues with data integrity, and compare results against historical data and established benchmarks.
• Summarize experimental results, contribute to the creation of technical reports, and maintain thorough and accurate experimental paperwork and laboratory notebook documentation.
• Participate as an extended team member in the planning and execution of experiments, collaborating effectively with colleagues in research and development and quality control.
• Perform assigned routine experimental techniques and laboratory processes in accordance with the requirements of the functional area and established SOPs.
• Perform equipment maintenance as needed and assist in generating and executing equipment Installation Qualification (IQ) and Operational Qualification (OQ) protocols.
• Adhere to all Environmental Health and Safety (EH&S) procedures and general housekeeping SOPs to maintain a safe, clean, and compliant laboratory environment.
• Comply with site- and department-specific procedures related to record keeping, use of log books, materials receiving, and inventory control.
• Complete time records accurately and report project time allocation in accordance with departmental requirements.
• Participate in implementing solutions for laboratory and infrastructure improvements to enhance efficiency, safety, and data quality.
• Demonstrate a primary commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all documented quality processes and procedures.
• For individuals with supervisory responsibilities, ensure appropriate resources such as personnel and tools are maintained to support Quality System compliance, and promote a work environment that upholds the Quality Policy and Quality System.

Additional Skills & Qualifications

• Bachelors degree (BA/BS) in Biology, Chemistry, or a related Engineering field.
• At least 2 years of experience in the medical device industry.

Work Environment This position is based onsite at a laboratory facility and operates on a first-shift schedule, typically from 8:00 a.m. to 4:30 p.m.

Job Type & Location

This is a Contract position based out of Maple Grove, MN.

Pay and Benefits

The pay range for this position is $31.00 - $36.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Application Deadline

This position is anticipated to close on Oct 30, 2026.

Workplace Type

This is a fully onsite position in Maple Grove,MN.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Reasonable Accommodation

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI)

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.