HIRING Biomanufacturing Associates! Medix Life Sciences is the fastest growing staffing organization specializing in Clinical Research and Life Sciences placements for all the major health systems and research organizations throughout the country. Medix is looking for an Associate's or Bachelor's Degree in Life Sciences and at least 1+ year of biologics industry experience.
Requirements:
Degree: Associates or Bachelors in a Life Sciences discipline
Associate I: 1 - 2 years of biologics industry experience, MFG Associate II: 2 - 4 years of biologics industry experience, MFG Associate III: 5 - 7 years of biologics industry experience
Knowledge of biotechnology operations such as, Aseptic Filtration Systems, Fermentation Process, Inoculation Process, Chromatography Columns, TFF step etc.
Position Summary: Location: Chicago, Illinois 60616 Pay: 24-40/hr depending on experience Hours: rotating shifts *SIGN ON BONUS* *RELOCATION ASSISTANCE FOR OUT OF STATE CANDIDATES*
Position Description:
The Manufacturing Associate will be responsible for the manufacturing of Biotechnology
products for clinical and commercial human use. Employees employ aseptic techniques while working in controlled and classified environments, some of which require complete aseptic gowning. Must comply with company policies, procedures (SOP), FDA current Good Manufacturing Practices (cGMP), and any other government requirement.
Will be assigned to the daily operations, working with:
Weighing and dispensing of material
Filtration systems
Inoculation of mammalian or cytokines cells
Fermentation and harvest
Chromatography columns and 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 accurately and in a timely manner.
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 or events that arise during the shift 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.
Performs other functions as required or assigned
Complies with all company policies and standards
Qualified candidates are encouraged to apply!We would love to discuss these positions with you further!