Biologist Entry Level Jobs in Minnesota (NOW HIRING)

Description

This position will consist of transforming the frozen plasma into freeze-dried plasma. They will be walking into the freezer to grab the frozen plasma and put it into a machine that will thaw it out. Once this is completed they will transfer the liquid plasma into another bag to put it into the lyophilizer for 7 days to extract all of the moisture to turn it into a freeze dried substance. They will repackage the plasma in the kitting room after that. Every unit is tracked in a BECS system, so attention to detail and experience in a GMP environment is needed. When they are not spending their time in the cleanroom they will be reviewing procedure and redlining the production procedure to continuously improve it. At this point in time the majority of their time is spent working at the desk. • Champion a safety driven culture. Ensure compliance with all safety and environment regulations. • Manufacture, inspect, and package products following written processes. • Work at a pace that meets, or exceeds, established time standards while making quality product. • Build, inspect and package product following written procedures and using applicable equipment to perform basic visual, dimensional, time and documentation checks, while meeting established timed standards and production goals. • Identify quality issues or workmanship deficiencies related to equipment, assembly and inspection processes, materials, sub-assemblies, and manufacturing environment. • Comply with GMP requirements by maintaining individual training records, completing data entry in production records in a timely and accurate manner, and adhering to documented manufacturing practices and procedures. • Maintain a clean, safe and organized work environment. • Comply with all policies and procedures. • Cross-train across multiple product lines following the Teleflex program. • Perform other duties as assigned.

Skills

Production, Gmp, documentation review, gdp, Laboratory, Sop, Biology

Top Skills Details

Production,Gmp,documentation review,gdp

Additional Skills & Qualifications

GMP understanding (6+ months) GDP Experience (6 months. we want someone that can document correctly-verify with references) Understands how to follow SOPs Computer Literate (they will be logging information into a BECS system) 6+ months of relevant experience required – Biologics, Pharmaceuticals or Medical Devices Experience in a highly regulated environment preferred. Must be able to read and understand policies, procedures and processes written in English Able to communicate effectively through oral and written communication Responsible for accurate documentation in a highly regulated environment Able to think critically and make decisions independently Ability to train operators to applicable manufacturing procedures and train on use of production equipment. Capable of multitasking and switching between tasks frequently Ability to sit frequently, stand, walk, bend, occasionally lift and go in/out the walk-in freezer Demonstrated ability to achieve quality and labor time targets required Requires Hepatitis B shot series or waiver

Experience Level

Entry Level

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

The pay range for this position is $25.00 - $25.00/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 Maple Grove,MN.

This position is anticipated to close on Aug 18, 2026.

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.

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