Category

Description

• Assist in the manufacture of pharmaceutical parenteral products for use in clinical studies. Operations are carried out in a cGMP compliant manner with strict adherence to OSHA safety requirements, SOP’s and batch records.
• Unit operations include but are not limited to parts washing, parts preparation & sterilization, buffer preparation, active formulation, integrity testing of equipment & product filters, visual inspection and general maintenance and cleaning of the manufacturing area.
• Responsible for equipment setup and operation, batch execution including completion of associated batch documentation and equipment logs, equipment cleaning and equipment storage.
• Entry of data into computer terminals when required.
• Position may include handling of potent compounds.
• Perform in accordance with specific instructions, all operations necessary for the operation and cleaning of equipment used for the above mentioned operations.
• Alert supervisor of any irregularities in procedures or equipment operation.
• Perform preventative maintenance as required.
• Adheres to the established manufacturing schedule for all assigned batches from start to completion

• A two year Associate Degree in Science related to Pharmaceutical Development or equivalent field. In lieu of a two-year degree, a minimum of four years’ working experience GMP pharmaceutical manufacturing or related field.
• Proficiency in the use of computer programs/systems is essential.

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