GenScript/ProBio
biotechnology
(Sr)Technician,DownstreamProcess
Neural analysis suggests this role is
optimal for Mid+ candidates.
“(Sr) Technician, Downstream Process at GenScript/ProBio. Skills: microbial purification, mammalian purification, chromatography, tangential flow filtration (TFF). Performs routine microbial and mammalian purification. Monitors chromatography and tangential flow filtration (TFF) systems during processing”
Industry & Context.
recognizes deviations from procedures and raises issue to management for resolution
maintains clean room environment to comply with regulatory requirements
What They're Looking For.
Must Have
Demonstrated ability to follow written instructions and procedures, Demonstrated ability to pay strict attention to detail, Proficiency with Microsoft Office, Excellent verbal and written communication and skills, Ability to work collaboratively as part of a team, in a fast-paced, matrixed, team environment consisting of internal and external team members, 0 – 5 years relevant experience (with Bachelor's degree), minimum of 3 years relevant experience (with Associate's degree), minimum of 7 years relevant experience (with High school diploma)
What You'll Do.
Performs routine microbial and mammalian purification
Monitors chromatography and tangential flow filtration (TFF) systems during processing
Weighs and checks raw materials
assembles process equipment
and monitors processes
Completes work instructions and maintains clean room environment to comply with regulatory requirements
Operates all production equipment in assigned functional area such as single use chromatography systems
chromatography columns
other disposable Bioprocess equipment
and solution preparation equipment as per written procedures
Authors solution preparation Master Batch Records (MBRs) by transferring technical information from scientific and development documents
Proposes and routes revisions to existing SOP’s for functional area equipment
Works to become proficient on common bioprocessing equipment
Conducts Safety and GMP self-auditing walkthroughs
documenting observations for assignment and closure dates
Tracks and ensures closure of observations
Logs and submits samples in Laboratory Information Management System (LIMS); tracks results and compiles data
Reviews own work for completeness on executed Master Batch Records (MBRs)
Coordinate the tracking and return of executed records to Quality department for review
Coordinates with Logistics to ensure needed materials are delivered to the production area timely
Monitors future needs against material supply to alert Logistics of shortfalls
Performs other tasks and assignments as needed and specified by management
How You'll Work.
Team & Collaboration
Ability to work collaboratively as part of a team, in a fast-paced, matrixed, team environment consisting of internal and external team members; Coordinates with Logistics to ensure needed materials are delivered to the production area timely; Monitors future needs against material supply to alert Logistics of shortfalls
Communication Scope
Excellent verbal and written communication and skills
Full Job Description
About GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio: ProBio, a subsidiary of GenScript, is a global CDMO offering end-to-end services from discovery to GMP for plasmids, antibodies, and cell recognizes deviations from procedures and raises issue to management for resolution. Adheres to current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs). Performs routine microbial and mammalian purification. Monitors chromatography and tangential flow filtration (TFF) systems during processing. Weighs and checks raw materials, assembles process equipment, and monitors processes. Completes work instructions and maintains clean room environment to comply with regulatory requirements Operates all production equipment in assigned functional area such as single use chromatography systems, chromatography columns, other disposable Bioprocess equipment, and solution preparation equipment as per written procedures. Authors solution preparation Master Batch Records (MBRs) by transferring technical information from scientific and development documents. Proposes and routes revisions to existing SOP’s for functional area equipment. Works to become proficient on common bioprocessing equipment. Conducts Safety and GMP self-auditing walkthroughs, documenting observations for assignment and closure dates. Tracks and ensures closure of observations. Logs and submits samples i
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