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Biomanufacturing Downstream Senior Associate

Madison, WI

Posted: 12/22/2020 Job Number: JN -122020-12328

Job Description

cGMP Biomanufacturing Downstream Senior 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: cGMP Biomanufacturing Downstream Senior Associate
  • Location: Madison, Wisconsin
  • Industry: Pharmaceutical and Biologics
  • Hours: 3rd shift: Wed- Sat, 10pm-8am
  • Salary: Up to $29.90/hr. depending on skill set
  • Employment Type: Up to 6 month contract
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.

Responsibilities:
  • Purify proteins of interest by utilizing different types of chromatography resins to either A) Bind the protein of interest and wash away impurities or B) bind impurities and collect the protein of interest.
  • Once the protein is free of impurities it is filtered to remove any remaining virus from US processing and concentrated to the correct concentration as well as formulated to the client s specific request. Finally, it is dispensed into appropriate containers and shipped out.
  • The Sr. Associate is expected to be fully trained on all operations, participate in training/mentorship of junior team members, and act as a project lead with some guidance (assisting Supervisor in project scheduling and attending client calls).
  • Advanced tasks may include review of Batch Records and other controlled documents.
  • The Downstream team provides an excellent opportunity for those interested in building a foundation of knowledge in the chromatography focused aspect of biologics production, as well as protein purification process as whole.
Qualifications
  • Minimum of high school diploma or GED
  • Minimum two years within a cGMP environment; Pharmaceutical, Biologics, Cell Gene or related industry knowledge
  • Experience with chromatography focused aspect of biologics production
  • Experience weighing raw material and staging for manufacturing
  • Ability to stand on your feet up to 10 hour shifts and commit to schedule
ADA/EOE
Search words: Pharmaceutical, FDA, cGMP, manufacturing, production, buffers, solutions, mixing, weighing, solution prep, blending, compounding, biologics
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