Posting date: February 20, 2013 |
Perform the functions necessary to assemble raw materials and subassemblies into finished bulk product according to cGMP and ISO.
Follow specific work instructions to manufacture bulk products, subassemblies, buffers, etc.
Perform calculations to determine specifications, bulk volumes, raw material quantities, etc.
Weigh and measure raw materials, select and set up processing equipment and instrumentation.
Interface with the Quality Control Laboratory to determine testing requirements, submit testing samples, and evaluate test results.
Ensure products are manufactured in accordance with work instructions, cGMP and ISO regulations.
Maintain accurate formulation records and process documentation in accordance with cGMP and ISO regulations.
Research previous lots/batches and plot trends.
Reconcile job materials.
Acknowledge and adhere to company policies and procedures.
Monitor equipment in the Formulation area.
Other duties as appropriate to position and assigned by the company.
Requires a Bachelor’s Degree in a Life Science or an equivalent combination of education and experience.
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