Document Control Scientist

Responsibilities

• Transfer and reformat SOPs related to immunoassay development.
• Utilize existing documentation to integrate into new SOP templates.
• Ensure quality assurance through data entry and document accuracy.
• Engage in formulation processes including weighing materials and measuring pH.
• Support documentation projects related to site transfer.

• Formulation
• Laboratory skills
• Chemistry
• GMP experience
• Data entry
• Quality assurance expertise

• Bachelor's degree in life science (chemistry, biology, biochemistry, microbiology).
• 6+ months of experience in a GMP environment.
• 6+ months of experience writing SOPs.
• Experience in production formulation including weighing materials and using a spectrophotometer.
• 3+ months of experience with immunoassay manufacturing.
• Knowledge of writing CAPAs, supplier notifications, and change orders.
• Familiarity with inventory management systems.

This position is a full-time, desk-based role, operating Monday through Friday on the first shift with start times between 6 am and 9 am for an 8.5‑hour workday. The team has recently undergone reorganization and focuses on new product introduction, site transfer projects, CAPAs, maintenance requests, and supplier notifications.

This is a Contract position based out of Minneapolis, MN.

The pay range for this position is $28.00 - $30.00/hr.

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)

This is a fully onsite position in Minneapolis, MN.

This position is anticipated to close on Jan 5, 2026.

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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccom (%20actalentaccom) for other accommodation options.