Downstream Associate Scientist - Alphanumeric Systems, Inc.
King of Prussia, PA
About the Job
Alphanumeric is hiring a Downstream Associate Scientist to work in Upper Merion, King of Prussia, PA with our client of 20 years committed to improving lives through medical and pharmaceutical advancements.
Must be able to work on a W2
Hourly Pay: $27.38
Hourly Pay: $27.38
*Downstream Role
o Work Shift = 1st shift standard day shift (i.e. Mon-Fri; 40 hrs/wk; 8 hrs/day; 7:30 AM - 4:00 PM) with early morning/evening and weekend work required occasionally, as needed
o 100% onsite work
o Duration = One year from start date, with possible extension to 18 months total
o *PAPR screening will be required after hire & will require completion of US Medical Clearance/Surveillance needed for CW to be completed for Respirator Use (Non-SCBA (OSHA regulated))
o Work Shift = 1st shift standard day shift (i.e. Mon-Fri; 40 hrs/wk; 8 hrs/day; 7:30 AM - 4:00 PM) with early morning/evening and weekend work required occasionally, as needed
o 100% onsite work
o Duration = One year from start date, with possible extension to 18 months total
o *PAPR screening will be required after hire & will require completion of US Medical Clearance/Surveillance needed for CW to be completed for Respirator Use (Non-SCBA (OSHA regulated))
Top Skills for Candidate:
o Ability to work in highly matrixed organization.
o Ability to multi-task within a multi-functional team environment.
o Able to troubleshoot.
o Capable of following written instructions and have clear written communication skills as well as computer literacy.
o Familiar with basic scientific principles and have experience in routine bench work and/or instrumental analysis.
o Ability to author, revise and/or support SOP's, change controls, deviations.
Summary & Key Words:
o Preparation of buffer solutions, chromatographic separation, filtration and concentration operation, etc.
o Completing daily manufacturing tasks per standard operating procedures and batch document instructions.
o Documenting all manufacturing activities clearly and accurately.
o 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 CIPs
o Work with hazardous materials under the appropriate safety procedures
o Performs other functions as necessary or as assigned.
o Ability to work in highly matrixed organization.
o Ability to multi-task within a multi-functional team environment.
o Able to troubleshoot.
o Capable of following written instructions and have clear written communication skills as well as computer literacy.
o Familiar with basic scientific principles and have experience in routine bench work and/or instrumental analysis.
o Ability to author, revise and/or support SOP's, change controls, deviations.
Summary & Key Words:
o Preparation of buffer solutions, chromatographic separation, filtration and concentration operation, etc.
o Completing daily manufacturing tasks per standard operating procedures and batch document instructions.
o Documenting all manufacturing activities clearly and accurately.
o 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 CIPs
o Work with hazardous materials under the appropriate safety procedures
o Performs other functions as necessary or as assigned.
Basic Qualifications:
o Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field.
o Familiarity with protein purification process operations and Good Manufacturing Practices (GMP) regulations.
o No experience required
Preferred Qualifications:
o 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.
o 1+ years of cGMP experience
o Knowledge of cGMP guidelines and standards.
o Knowledgeable of: Cytiva platform of purification equipment and Unicorn software
o Proficiency in executing standard procedures required in addition to some non-routine work.
o Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field.
o Familiarity with protein purification process operations and Good Manufacturing Practices (GMP) regulations.
o No experience required
Preferred Qualifications:
o 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.
o 1+ years of cGMP experience
o Knowledge of cGMP guidelines and standards.
o Knowledgeable of: Cytiva platform of purification equipment and Unicorn software
o Proficiency in executing standard procedures required in addition to some non-routine work.
Source : Alphanumeric Systems, Inc.
