A career at Resilience is more than just a job - it's an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made . We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit www.resilience.com This position will require working in various Controlled/Non-Classified areas. The Technician performs a variety of manufacturing tasks (operates equipment, performs visual, cosmetic, and physical inspection, line clearances, OEE data collection and completes batch record entries) and supports improvement activities (5S, participate in problem-solving and Kaizen events, manual data collection) in accordance with cGMPs. Primary Responsibilities * Perform the duties of using the approved tools to create defect units that will be used in Inspection defect kits. * Conduct evaluations on other team members for training qualifications. * Perform cleaning and housekeeping for assigned areas as required to maintain a cGMP environment. * Perform GMP documentation entries. Maintain records and/or logs as required in the performance of job responsibilities. This will include mathematical computation where needed. * Knowledge of product security controls and kit reconciliation. * Be familiar with job-related safety procedures and hazards including PPEs, ergonomics, human safety, material handling, waste handling, chemical handling, and spill controls. Report all discrepancies to process Manager. * Perform work requirements in a responsible manner, in accordance with SOPs, cGMPs and established safety procedures in accordance with OSHA requirements and guidelines. Be familiar with "Material Safety Data Sheets" for area chemicals. * Obtain knowledge to be able to print off SOP's/Forms via ECMS. * Review process documents such as operational SOPs, forms and batch records for accuracy. Identify and provide suggestions for process improvement while maintaining quality and cGMP compliance as opportunities arise. * Assist with creating and maintaining visual inspection standards. * Assisting with investigations and resolving visual inspection issues. * Collaborating with cross functional teams to address any challenges. * Operate defect lab equipment in accordance with EHS and Quality standards. * Perform all other assigned duties with minimal supervision under the direction of the Manager. * Capable and motivated to learn new skills and develop new capabilities on an on-going basis to contribute to the success of the Inspection Team. * Ability to work effectively in a team environment. * Candidate should possess the ability to work in and adapt to a changing/demanding environment. * Some overtime may be required with minimal advance notice to support business needs. Other Responsibilities * Support lean activities and process improvement work such as performing 5S in the work area, participating in problem-solving, and manual tracking of performance data for OEE and process improvement analysis. * Perform all other assigned duties with minimal supervision under the direction of the Manager or designee as needed. Optional Training / Responsibilities * Obtain cold room training/access to be able to transfer materials in and out of the cold rooms. * Take proper training to become certified trainer on assigned process tasks. Minimum Requirements: * Prior experience in a pharmaceutical or cGMP regulated environment * Must have the ability to effectively understand, read, write, communicate and follow instructions in the English language. * Good