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Performs microbiology department related raw material, in-process, and finished product testing according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques.
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Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines. With donation centers and team members throughout the U.S., Octapharma Plasma, Inc. collects plasma to create life-saving medicines for patients worldwide.
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Monitors filling operations in compliance with company policies/procedures, FDA and cGMP regulations. Monitors all filling areas and personnel for adherence to all cGMP, SOP's and safety regulations.
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Specialized medical or phlebotomy training. Team lead/Supervisor experience. Our strong growth is creating great learning and career development opportunities throughout our company, and especially our donation centers.
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Follow Standard Operating Procedures, safety, health, and cGMP Guidelines. Notify Laboratory Management of laboratory problems. In addition, the Laboratory Technician will be responsible for ordering, inventory of materials, and tracking maintenance and calibration of all laboratory equipment.
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Knowledge and experience with cGMP, QA/QC fundamentals, SOP, Manufacturing, OSHA and DEP/EPA as they relate to the pharmaceutical industry is required. · Maintains regulatory records and completes all required documentation in compliance with cGMP, FDA, USP and pharmacy state board regulatory guidelines.
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Employee will carry out manufacturing practices in a cGMP biotechnical facility. Tissue Processing Technician I is the entry level into the Tissue Processing Technician job group. Every day, more than 4,000 of us are challenging what's possible and making headway to help improve outcomes.
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