Your Biopharmaceutical Development and Manufacturing Partner

Manufacturing Senior Technician

  • This position will support production related activities in the cGMP Manufacturing Core according to established procedures at the Medical Counter Measures (MCMs) Advanced Development and Manufacturing Facility in Alachua (Florida). 
  • Perform upstream related activities including Cell culture at small/large scale using various cell lines, Cell transfection, Media and buffer preparation, Bioreactor and Fermentor based production. 
  • Perform downstream related activities including Chromatography purification, Centrifugation and Ultracentrifugation, Ultrafiltration/Diafiltration, Viral Clearance.
  • Write Standard Operation Procedures, Change Control, Deviations.
  • Properly disinfect and stage materials into production rooms before the production campaigns.
  • Identify and order equipment. Oversee equipment installation, qualification and routine maintenance.
  • Write and/or review Production batch records and review executed records.
  • Write raw material specifications, research and source material and lab wares. 
  • Write production reports when necessary.
  • Perform change-over cleaning in the manufacturing core and other production rooms.
  • Perform activities to support production campaign such as preparation of tubing assemblies, autoclave, material request and transfer into production room.
  • Adhere to safe working practices.
  • Provide other assistance as needed to the Manufacturing Supervisor or Manager.
  • Meet with Manufacturing Supervisor and/or Manufacturing Manager at least on a weekly basis to discuss goals, planning, progress.

Minimum Educational Requirements for Competency

  • Possess a B.S. (Biology, Microbiology, Molecular Biology, Virology, Immunology, Chemistry, Engineering, Biochemistry, Material Science or related field) with a minimum of 3 years of work experience (cGMP experience preferred) 
  • OR A.S diploma and a minimum of 5 years of cGMP manufacturing experience.
  • Ability to document work clearly and accurately. Detail oriented.
  • Must have basic computer skills and familiar with Word, Excel and Powerpoint.
  • Legible writing skills. Ability to maintain accurate records.
  • Communication and organization skills in teamwork environment.
  • Experience working as a team member sharing responsibilities is desired.
  • Previous work experience in cGMP environment is highly desired.
  • Ability to work independently and within the manufacturing group to complete assigned tasks.
  • Flexibility, Self-motivation, efficiency and responsibility, hard working.

This position will be based in Alachua, FL.

To apply submit your resume to with the position in the subject line.



Nanotherapeutics is an equal employment opportunity for all without regard to race, color, religion, sex, age, national origin, disability, or any other characteristic protected by applicable law. If you need assistance in applying for a position, please contact us through or call 386-462-9663.

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