Supervisor, Manufacturing & Process Execution (Nights)

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 Position Summary The Supervisor is a leader for the Process Operation (Formulation & Parts Prep). In this capacity, the Supervisor manages the Process / Package Operation to produce high-quality product in accordance with the PET operating strategy. As a responsible leader for the operation (potentially with another Supervisor), this must be done while maintaining effective employee relations and compliance with cGMP, other regulatory, and SOX requirements, as well as SHE obligations and Resilience standards. Job Responsibilities Provides direction to PET personnel in the efficient use of equipment and materials to produce quality products in accordance with the PET Plan or Rhythm Wheel. Responsible for all PET activity, including coordination of support staff, scheduling, and improvement. Promotes the use of safe work practices during all aspects of production and ensures all external and Resilience SHE standards are met on a daily basis. Accountable for training PET personnel on equipment, processes, and Standard Operating Procedures. Partners with the PET Coach to develop training plans and assists in providing resources for training. Ensures cGMPs are used and followed during production so that all FDA and international regulations are met. Responds to monthly internal audit observations. Promotes a positive work environment by effectively administering Resilience Human Resources policies and procedures, including Performance Management, communicating information to employees, and responding to their concerns. Ensures proper documentation practices are maintained consistently to company standards in manufacturing documents, training documentation, production logs, etc. Generates reports for deviations, assists in investigations, and recommends and implements solutions to resolve deviations. Approves deviation investigations as appropriate. Responds to product defect notifications. Authors, reviews, and approves Standard Operating Procedures and other documents to ensure integration of cGMPs and improve process efficiencies. Promotes and encourages continuous improvement in efficiency, quality, production, and safety using team-driven processes, key performance indicators, and recognition and rewarding of high performance. Collaborates with OE Engineers and PET Engineers to optimize process performance. Participates in the design, selection, installation, and qualification of new equipment, facilities, and processes. Reviews, approves, and implements change controls. Provides career development…