Manufacturing Associate

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 Job Type & Location This is a Contract position based out of Maple Grove, MN. Pay And Benefits 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) Workplace Type This is a fully onsite position in Maple Grove,MN. Application Deadline 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. 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 process due to a disability, please email actalentaccommodation@actalentservices.com 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.