Operating manual and automated equipment to perform Microbial Fermentations, Down Stream Purifications, Active Pharmaceutical Ingredient (API) or fine chemical manufacture.
Controlling processes from start-up to shutdown, including unit operations of microbial growth, expression, recovery, filtration, chemical synthesis, and purification.
Handling of hazardous materials, including acids, bases, solvents, potent compounds, biologics and APIs safely and properly.
Performing process sampling and testing including pH, conductivity, spectrophotometry, osmometry, densometry, aseptic sampling and streak plating, etc.
Collaborating with other departments on process and equipment training for successful completion of manufacturing batches.
Preparing shift summaries and updating excel spreadsheets with key performance and quality indicators.
Providing feedback to influence continuous improvements during the review and revision of Standard Operating Procedures and other process documentation.
Participating in BIOVECTRA's quality management system, focusing on the batch production records, work instructions, adherence to policies and standard operating procedures at all times.
Assisting with housekeeping, equipment cleaning, general warehousing, material staging, and tanker operations as required.
Qualifications
0-2+ years' experience working in a cGMP or regulated environment (food, aerospace, pharmaceuticals) is a plus.
Excellent attention to detail.
Proficient communicator, both written and oral.
Ability to work independently with minimal supervision.