Laboratory Technician

Job Title : Downstream Associate ScientistLocation: King of Prussia, PA, 19406Duration: 12 Months (One year from start date, with possible extension to 18 months total)100% OnsiteBachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific fieldPlease also note that there is a CLIENT holidayshutdown occurring shortly after the identifiedspecified start date, where remote work may or may not be available for the new hires.Downstream Role:Work Shift = 1st shift standard day shift (i.e. Mon-Fri; 40 hrswk; 8 hrsday; 7:30 AM - 4:00 PM) with early morningevening and weekend work required occasionally, as needed100% onsite workDuration = One year from start date, with possible extension to 18 months total*PAPR screening will be required after hire & will require completion of US Medical ClearanceSurveillance needed for CW to be completed for Respirator Use (Non-SCBA (OSHA regulated))Basic Qualifications:Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field.Familiarity with protein purification process operations and Good Manufacturing Practices (GMP) regulations.No experience requiredPreferred Qualifications:Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field with 1+ years of direct purification experience in a Pilot Plant or manufacturing setting.1+ years of cGMP experienceKnowledge of cGMP guidelines and standards.Knowledgeable of: Cytiva platform of purification equipment and Unicorn softwareProficiency in executing standard procedures required in addition to some non-routine work.Top Skills for Candidate:Ability to work in highly matrixed organization.Ability to multi-task within a multi-functional team environment.Able to troubleshoot.Capable of following written instructions and have clear written communication skills as well as computer literacy.Familiar with basic scientific principles and have experience in routine bench work andor instrumental analysis.Ability to author, revise andor support SOP's, change controls, deviations.Summary & Key Words:Preparation of buffer solutions, chromatographic separation, filtration and concentration operation, pleting daily manufacturing tasks per standard operating procedures and batch document instructions.Documenting all manufacturing activities clearly and accurately.Ensures all production activities are completed in a safe and compliant manor. Maintain and prepare high quality documentation. Dispense large and small amounts of raw materials Perform CIPsWork with hazardous materials under the appropriate safety proceduresPerforms other functions as necessary or as assigned.

Created: 2024-11-06