Sr Associate, CGMP Biomanufacturing

Madison, WI

Posted: 03/05/2021 Industry: R&D Scientist Job Number: JN -032021-12644

Job Description

Manufacturing Associate

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
  • Title: Sr Associate, CGMP Biomanufacturing
  • Location: Madison, WI
  • Industry: Pharmaceutical
  • Hours: Sun-Wed 6am-4pm 1st Shift (AM) Wed-Sat 6am-4pm 1st Shift (AM) Sun-Wed 2pm-12am 2nd Shift (PM) Wed-Sat 2pm-12am 2nd Shift (PM) Sun-Wed 10pm-8am 3rd Shift Wed-Sat 10pm-8am 3rd Shift
  • Salary: $18.50 - $29hr Determined by Shift (Paid Weekly - Benefits Available)
  • Employment Type: Long Term Contract to Hire
Environment: This client manufactures thousands of pharmaceutical, biologic, consumer health and beauty products utilizing superior and innovative drug delivery technologies to improve their value to patients and consumers. Our customer believes in a Patient First culture putting patients at the center of their work to ensure the safety, reliable supply and optimal performance of our products.

Job Scope:

The cGMP Biomanufacturing group is responsible for current Good Manufacturing Practices (cGMP) production activities, including master/working cell bank production, upstream cell culture, downstream protein purification, and mRNA therapeutics production. This is an entry level position and is a great starting point to acquiring the skills and training required for a cGMP Biomanufacturing environment. This role is primarily responsible for performing basic manufacturing operations in a clean room environment according to established procedures with support and supervision.

This is a temp-to-permanent, full-time position located in Madison, WI. It is an hourly role, eligible for overtime. The work schedule would be 4 days/week x 10 hours/day. Multiple teams and shifts available! Base pay + shift differential.
Common titles can be:
Manufacturing Associate, Manufacuting Technician, Biotechnology Technician, Biomanufacturing Associate, Lead Technician, Environmental Monitoring Technician, Quality Control Technician, Quality Assurance Technician, Process Technician,
Essential Functions:
  • Performs aseptic techniques within a clean room environment.
  • Executes and properly documents cGMP Biomanufacturing activities.
  • Operates cGMP Biomanufacturing equipment, including pH/conductivity meters, mixing tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances, and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH).
  • Supports Biomanufacturing staff with proper completion of Standard Operating Procedures (SOP), Batch Production Records (BPR) and Job Aid (JA) as applicable.
  • Specific duties will vary by team:
  • Solution Prep Weighs/dispenses chemicals or components and stages materials for solution preparation.
  • Upstream Manufacturing Performs basic cell culture work, including but not limited to working inside of a biosafety cabinet, cell counting, performing manipulations of required cell cultures in an ISO 5 environment, and analyzing cell culture samples.
  • Downstream Manufacturing Performs column, membrane adsorption and size-exclusion chromatography, including viral reduction and filtration steps. Performs routine protein purification analytics, including protein concentration, pH and conductivity.
  • mRNA Therapeutics Prepares medias and solutions. Operates Biomanufacturing equipment to perform mRNA transcription, reaction chemistries, and tangential flow filtration.

  • Bachelor s in Biotechnology or related field with 0-2 years relevant experience
  • Associate s Degree/Certificate with 0-4 years relevant experience
  • High School Diploma or equivalent with 1-5 years relevant experience

  • Clean room, aseptic technique, and/or general lab equipment experience.
  • cGMP, Good Documentation Practices (GDP) and Good Laboratory Practices (GLP) knowledge.
  • Following standard operating procedures (SOP).


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