Manufacturing Associate
Job Description
The Manufacturing Associate transforms frozen plasma into a freeze-dried product by operating specialized equipment in a cleanroom and highly regulated environment. This role combines hands-on processing of blood products with detailed documentation in electronic systems, continuous improvement of procedures, and cross-training across multiple product lines. The position offers the opportunity to contribute directly to an innovative, life-saving biologics product that will be used in critical care and emergency settings.
Responsibilities
Transform frozen plasma into freeze-dried plasma by following established processes and standard operating procedures (SOPs).
Retrieve frozen plasma from a walk-in freezer, load it into equipment to thaw, and transfer the liquid plasma into new bags for further processing.
Operate the lyophilizer to remove moisture from plasma over a multi-day cycle, monitoring the process and ensuring accurate handling and labeling.
Repackage and kit freeze-dried plasma in the kitting room according to written procedures and quality standards.
Track every unit of product accurately in the BECS system, ensuring complete and precise data entry in production records.
Manufacture, inspect, and package products by following written processes and using appropriate equipment for visual, dimensional, time, and documentation checks.
Work at a pace that meets or exceeds established time standards while consistently producing high-quality product.
Identify and report quality issues or workmanship deficiencies related to equipment, assembly and inspection processes, materials, sub-assemblies, or the manufacturing environment.
Comply with Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) requirements by maintaining individual training records and completing all documentation accurately and on time.
Review, follow, and help improve production procedures, including redlining documents to support continuous process improvement.
Maintain a clean, safe, and organized work environment in both the cleanroom and desk-based work areas.
Champion a safety-driven culture and ensure compliance with all safety and environmental regulations, policies, and procedures.
Cross-train across multiple product lines to support flexible manufacturing needs.
Train other operators on applicable manufacturing procedures and the proper use of production equipment, as needed.
Communicate effectively with team members and leadership regarding production status, issues, and improvement opportunities.
Meet quality and labor time targets while multitasking and switching between tasks as required.
Perform other duties as assigned to support production, quality, and continuous improvement goals.
Essential Skills
At least 6 months of experience working under Good Manufacturing Practice (GMP) requirements.
At least 6 months of Good Documentation Practice (GDP) experience with proven ability to document accurately and completely.
Minimum 6 months of relevant experience in biologics, pharmaceuticals, or medical devices.
Understanding of and adherence to standard operating procedures (SOPs).
Experience in a highly regulated environment.
Strong computer literacy, including the ability to log information into electronic systems such as a BECS system.
Ability to read and understand policies, procedures, and processes written in English.
Effective oral and written communication skills.
Demonstrated responsibility for accurate documentation in a highly regulated environment.
Ability to think critically and make decisions independently within defined procedures.
Capability to train operators on manufacturing procedures and production equipment.
Ability to multitask and switch between tasks frequently while maintaining accuracy and quality.
Physical ability to sit frequently, stand, walk, bend, occasionally lift, and move in and out of a walk-in freezer.
Demonstrated ability to achieve quality and labor time targets.
Additional Skills & Qualifications
Experience with blood products, biologics, or similar materials.
Experience in cleanroom manufacturing environments.
Strong attention to detail and ability to follow complex written instructions.
Proven ability to learn quickly and adapt to new processes and technologies.
Interest in long-term growth into roles such as shift lead, team lead, engineering, regulatory, or quality.
Motivation to contribute to innovative, life-saving medical products used in military, hospital, and emergency settings.
Work Environment
This role is based in a cleanroom manufacturing environment that supports the production of highly regulated biologic products. When working in the cleanroom, you will spend the majority of your time on your feet and will be fully gowned in accordance with PPE and cleanroom SOPs. You will regularly move in and out of a walk-in freezer to retrieve frozen plasma and then work with specialized equipment, including a lyophilizer and electronic tracking systems such as a BECS system. A significant portion of the role also involves desk-based work reviewing, documenting, and improving procedures. The standard schedule is Monday through Thursday, 6:00 a.m. to 4:30 p.m. (four 10-hour days), with Friday work as needed. The environment emphasizes safety, cleanliness, documentation accuracy, and collaboration, and offers exposure to cutting-edge biologics manufacturing and opportunities for long-term career growth.
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 Jun 11, 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 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 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.
