Manufacturing Associate/Downstream Associate
Job Description & How to Apply Below
Location: False Pass
Job Description
Job title: Downstream Associate Scientist
Address
:
King of Prussia, PA - 19406
Contract: 1 Year (potential for extension)
Shift: Mon - Fri; 40 hrs/wk; 8 hrs/day
From 7:30 AM – 4:00 PM
Job Responsibilities- Preparation of buffer solutions, chromatographic separation, filtration and concentration operation, etc.
- Completing 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 CIP and SIP of product tanks
- Work with hazardous materials under the appropriate safety procedures
- Performs other functions as necessary or as assigned.
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.
Preferred 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 experience
- Knowledge of cGMP guidelines and standards.
- Knowledgeable of:
Cytiva platform of purification equipment and Unicorn software - Proficiency 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 and/or instrumental analysis.
- Ability to author, revise and/or support SOP's, change controls, deviations.
Position Requirements
10+ Years
work experience
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