Associate I, Manufacturing

Position Summary Responsible for performing processing/manufacturing activities of Human Transplant Tissues and devices in an FDA regulated GMP facility. Prepare processing solutions and storage media. Thaw and process frozen placental tissues into finished products. Perform production control on 100% of units manufactured, packaged and labeled. Initiate processing area set up and change over as needed. Conduct line clearance, equipment cleaning and facility cleaning as needed. Perform final product label creation, verification and labeling. Store final product in designated quarantine areas. Complete documentation (e.g. batch records, cleaning logs, etc.) for review. Maintain aseptic and/or neat work environments. Prepare disinfectant for equipment and Facility cleaning as necessary. Complete requisitions for quality control samples and submit to the designated lab for bio-burden testing. Provide information as needed to assist with investigations. Document/report equipment and facility problems and any potential deviation during processing. Skills & Abilities Essential Duty Definition: Excellent communication skills; fluent (oral/written) English. Ability to multi-task, setting priorities effectively to produce quality work in a fast-paced professional environment Communicates effectively and appropriately. Uses good judgment as to what to communicate to whom as well as the best way to get that accomplished. Speaks in a clear and credible manner, selecting the right tone for the situation and audience. Listens to others and allows them to make their point. Proficient in Microsoft software applications: Excel, Word, PowerPoint and Outlook. Familiarity with American Association of Tissue Banks, Good Manufacturing Practices (GMP), and Hazard Analysis a plus. Position Expertise/Qualifications High School Diploma, required Associate’s Degree in Biotechnology, Life Sciences, or Surgical Technology, preferred. 6 months experience in Biotech, laboratory or other science, required Manufacturing in a GMP environment, required Physical Requirements Sedentary work that generally requires sitting and/or standing #J-18808-Ljbffr BioTissue Ocular