Aaron Anders Email & Phone Number

Durham, NC, US

Raleigh, North Carolina, US

On site Lecturer supporting BBS-301 - Process Validation Science

Cambridge, MA, US

Durham, North Carolina, US

Durham, North Carolina, US

Durham, North Carolina, US

Durham, North Carolina, US

• Supervise a 4 member shift executing contract upstream manufacturing processes, 200L to 2000L scale.
• Make observations of aseptic technique and manufacturing operations, and ensure alignment with current company procedures.
• Assist with management of production/operation planning and scheduling.
• Troubleshoot and maintain manufacturing equipment.
• Prepare, review and approve technical documents including process transfer documents, batch records, solution records, process assembly records, equipment preparation records.
• Provide training on company procedures, operations, and equipment use.

Durham, North Carolina, US

• Support new process enrollment from process development to cGMP manufacturing and batch disposition.
• Execute investigations for all process deviations and associated CAPAs.
• Prepare, review and approve technical documents including process transfer documents, batch records, material item specifications and engineering specifications.
• Generate facility fit Bill of Materials (BOM) for accelerated material ordering to support enrolling projects.
• Develop process flow diagrams for facility fit and process design.
• Apply expertise in operational principles and bioprocessing equipment design to identify equipment to be used in new processes, and work with client, vendor, and Engineering to specify new equipment and equipment.

Durham, North Carolina, US

Perform deviation investigation and writing.Assist in the solution record and batch record generation, review, and approval process.Coordinate and perform cGMP upstream manufacturing operations.Ensure the effective use of material, equipment, and personnel while supporting production.Assist in execution of procedures for large scale cell culture and pilot.

Lead Engineer over an aseptic consolidation and blending process Provide technical support for a bulk sterilization facility including filtration, crystallization, drying, packaging, and aseptic consolidation and blending using a working knowledge of process procedures, DeltaV, SAP, Toldeo Scale Management, and LIMS.Perform investigations for process.

Assist in the qualification and start-up of a large scale microbial fermentation facility.Provide engineering support and assist with troubleshooting.Observe and document process procedures in order to help develop formal batch records and standard operating procedures.Execute and document CIP/SIP validation protocols.Assist with CAPA implementation and.

Develop project to research the effects of thermal processing and salt addition on aggregation and denaturation of whey protein isolate soluble aggregates.Analyze samples using solubility method, BCA assay, acid denaturation, centrifugation, turbidometer, size exclusion chromatography, and zeta potential.Compose lab notebook containing all methods used and.

Research Triangle Park, NC, US

Collect spectra for a number of process materials (gaskets, seals, tubing, etc.) using Raman and FTIR spectroscopy. Compile database of collected spectra to aid in identification of foreign particulate matter.Determine the best possible parameters to get representative data with the Raman spec for different material types.Practice good lab.

Used a working knowledge of the tutored subject to help develop independent learning. Meet with two to four students twice a week and developed a lesson plan suited to different learning styles. Encouraged good study habits and helped with development of studying plans. Achieved level two certification by finishing 20 hours training and 50 hours individual.

Master'S Degree, Biomanufacturing

B.S, Bioprocessing Science