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.
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 CIP and SIP of product tanks
o Work with hazardous materials under the appropriate safety procedures
o Performs other functions as necessary or as assigned.
Education:
Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field
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 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.