BioPharmaceutical Manufacturing Associate-1:

Responsibilities:

This person will be responsible for the aseptic processing of pharmaceutical components and products using cGMP standards while maintaining the production schedule. In this role, the responsibilities will include asceptic processing of components; aseptic processing of raw materials and upstream and downstream processing of pharmaceutical products; environmental monitoring of manufacturing facility; operation and basic troubleshooting of production equipment; maintain complete and accurate records of equipment logs, batch histories, computer output data, temperatures, pressures, and liquid levels; work effectively and efficiently in a team-oriented environment to keep manufacturing operations running smoothly; adhere to Standard Operating Procedures which conform to OSHA Standards, cGMPs and other established procedures during the manufacturing process to produce a quality product; The person will also be responsible to recommend or to initiate changes when and if necessary.

Requirements:

We require a minimum high school graduation degree or equivalent combination of education and relevant work experience. The person must be willing to work flexible hours and occasional overtime and be able to lift 30 lbs. and work extended hours while standing.