Minimum ·High School Diploma. ·One year experience in a production environment ·Demonstrated problem solving and troubleshooting skills ·Basic mechanical aptitude ·Basic computer skills ·Good interpersonal, communication and writing skills. ·Ability to perform duties with minimal supervision. ·Knowledge of cGMP’s. Preferred Three years experience as an operator in a production environment, pharmaceutical experience a plus This position is responsible for conducting rework of pharmaceutical products in a safe and efficient manner, complying with cGMP’s, SOPs, and site safety procedures. Major Responsibilities ·Must demonstrate ability to properly operate equipment (Visual Inspection System), perform equipment set-up/change-over/cleanups/purge, and troubleshoot equipment problems Supply equipment with components and product. Lifting requirements may be up to 30 lbs. Must be able to work other shifts, weekends, alternative schedules when production demands require ·Must understand and comply with cGMP’s, SOPs and site safety procedures. ·Perform detection system challenges on applicable equipment. ·Accountable for accurately documenting packaging and cleaning activities in Manufacturing Batch Records, Equipment Cleaning Logbooks. ·Perform on-line quality inspections and in-process testing (appearance, etc.) ·Share knowledge with co-workers for training purposes. ·Work effectively in teams to meet demand requirements. ·Identify areas for continuous improvement and efficiency improvements. ·Accountable for performance (OEE) and able to report status of equipment to affected personnel to ensure timely resolution to issues. (i.e. Facilitators, Engineers) Location: Wilmington, DE Compensation: 10-15/hr. This is a contract job. Principals only. Recruiters, please don't contact this job poster. Please, no phone calls about this job! Please do not contact job poster about other services, products or commercial interests. delaware