Technician I-Bio/Pharm Production - United States
|Technician I-Bio/Pharm Production|
|Elanco is a global research-based company that develops and delivers product and services to enhance animal health and production. We value innovation, both in scientific research and daily operations, and strive to cultivate a collaborative work environment for more than 7,000 employees worldwide. Founded in 1954, Elanco is a division of Lilly. Our worldwide headquarters and research facilities are in Greenfield, Indiana.|
|In this position, the incumbent will be trained in the set-up, operations and troubleshooting of the equipment in the production areas. Additional duties will include documentation of work and specific computer functions. Must integrate company initiatives such as BPE into work practices. Responsible for safely producing vaccines which meet all product specifications in accordance with current Good Manufacturing Practice standards. Interfaces with Quality Assurance, Production Planning and Maintenance. Contacts are primarily within immediate work unit and involve obtaining or providing information requiring explanation or interpretation. |
Accountabilities/ Indicators: 1-A). Perform duties associated with aseptic processes, weighing, measuring, counting, calculations, sampling, and verifications required for biological production processes in accordance with batch production records (BPR) and in compliance with current good manufacturing practice (cGMP) standards, all current safety standards and site procedures. 1-I). Outcome of review of compliance records and audits, as well as Deviation rate and Management assessment. 2-A). Understands and can perform basic operation of production equipment and ensures all equipment, instruments and production materials are released and available for use. Look up and perform transactions within the electronic inventory management system. 2-I). Overall equipment effectiveness, Deviation rate, and Management assessment. 3-A). To oversee production processes, cleaning, environmental monitoring and personnel and perform in-process batch quality checks per the written procedures. Knows and follows safety rules, wears appropriate safety equipment and maintains proper safety practices at all times.
3-I).Overall process effectiveness, Deviation rate, Accident Rate and Management assessment. 4-A). Basic computer skills to create and update standard operating procedures and write deviation reports, and to complete all training as assigned to include general company procedures, area procedures, equipment operation, computer operation, safety, GMP, BPE, and other as needed. 4-I). Workflow initiation and approval process to ensure all information is present and accurate, as well as Management assessment.
5-A). To generate or collect new ideas about workplace and processes. 5-I). Management assessment.