- Weighing and dispensing of materials used in pharmaceutical processing and manufacturing.
- Operating filtration systems
- Inoculation of mammalian or cytokines cells
- Fermentation and harvesting
- Use of chromatography columns and tangential flow filtration (TFF) operations.
- Responsible for in-process testing, such as: pH, Conductivity, Spectrophotometer, Osmometer, Cell count, etc.
- Prepares media and buffer solutions.
- Completes Batch Records and other cGMP documentation.
- Remove and dispose of soiled materials from the manufacturing area.
- Will assure that the manufacturing areas are maintained within the required conditions for clean room manufacturing.
- Will report all nonconformance to the Supervisor.
- Assists in the transfer of technology from Process Development to cGMP Manufacturing.
- Complies with all safety, cGMP and Company policies, practices and procedures.
- Minimum of Associate's Degree in Biology, Chemistry, Biotechnology, or a related scientific discipline.
- 1+ years of professional experience working in the pharmaceutical or biologics industry.
- Must be familiar with all 3 the following: Chromatography Columns, Fermenters or Bioreactors, and Tangential Flow Filtration (TFF) Operation.
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Manufacturing Associate - Chicago, United States - Sterling Engineering
Description
Title: Pharmaceutical Manufacturing Associate
Location: Chicago, IL
Hire Type: Contract-to-Hire
Overview:
Sterling has helped build careers for thousands of professionals like yourself. Our expert recruiters support you at every step in the process and as a Best of Staffing company, Sterling provides exciting work with exceptional employers across the U.S.
As a contract employee of Sterling, you are eligible to receive a Full Employee Benefits Package that includes paid time off, paid holidays, 3 medical plans to choose from, dental & vision plans, 401(k), and an Employee Stock Ownership (ESOP) plan.
Job Summary:
This is a Contract-to-Hire career opportunity with a nation-wide pharmaceutical manufacturer located in Chicago, IL. In this role, you'll use aseptic techniques to prepare solutions and operate pharmaceutical manufacturing equipment in a cGMP environment.
Job Duties:
Qualifications:
Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identify, national origin, disability, protected veteran status, or genetic information.