Manufacturing Supervisor-Night Shift - 2307014956W

　　DESCRIPTION/RESPONSIBILITIES:DescriptionKenvue is currently recruiting for a Night shift-Manufacturing Supervisor role. This position reports into the Senior Manager Packaging Operations and is based at Fort Washington, PA.

　　What will you do:Key Responsibilities:* Provide oversight to the manufacturing operations which includes, operate and troubleshoot, set up, adjust, repair and maintain the equipment and manufacturing processes.* Provide direction and make decisions within the scope of the role and responsibility for a variety of tasks included but not limited to quality and compliance, technical and people management. This includes, providing leadership to ensure adherence to all safety, environmental and quality policies and procedures.* Partner with the cross-functional teams to execute the production schedule, serve as back up to the Manager, assist management through change and transformation activities, be the Power User in the applicable systems, and understand the product family, product size and put-up, and product characteristics (color, viscosity) associated active and excipient.* Ensure quality and compliance by: attending Good Manufacturing Practices (GMP) training, adhering to compliance with procedures, exercising the highest level of integrity in the tasks performed, identifying/reporting and seeking correction for deviations, embracing a behavior of employee involvement and commitment to doing the job right the first time, and ensuring employees under your scope of responsibility are trained.* Be the Manufacturing Subject Matter Expert (SME) to understand the critical aspect of product, component and labeling requirements; be the point of reference for audits and act as SME.* Ensure adequate resources to support investigations, participate in/write or approve investigations, contribute and attend Environmental Health & Safety (EHS) programs, promptly communicate deficiencies to management, document all activities per the GMP requirements, take necessary action to eliminate and immediately address safety hazards, communicate observed unsafe behaviors, and coordinate efforts in case of emergency- spill, fire etc.* Extract, enter all commitments from regulatory documents, internal audits into the commitment tracking systems. Monitor and follow up to ensure timely completion of all commitments.* Approve Standard Operating Procedures (SOP) and relevant quality documentation. SME and responsible for review and sign off of relevant documentation per the function (i.e. manufacturing) as required by the quality process in the execution of the relevant work.* Perform/assist in the completion and documentation of the process steps as per the documentation directives; complete visual verification of the process and document these steps in the appropriate system.* Proactively identify, evaluate, and prioritize opportunities for continuous improvement; drive implementation of continuous improvement actions and kaizen events, act as a champion for Process Excellence/Lean methodology and support the team in the application these concepts.* Responsible to develop, train and educate the direct report and provide resources and support to ensure that they can execute successfully and in a compliant manner their goals and objectives.* Provide feedback to site management and support strategic/tactical plans in alignment with site's mission and plans.

　　Hours are 6pm-6:00am on a 2-2-3 Schedule

　　QualificationsWhat We Are Looking ForRequired QualificationsEducation: Professional, vocational, or technical certification or Associates degree is required. Bachelor's Degree in Engineering, Science, or Business is preferred

　　A minimum of six (6) years of relevant experience in a regulated manufacturing environment or four years with a Bachelor's degreeProven ability to interact, motivate, and lead individuals in a manufacturing environ ent.Strong Microsoft Office skills, including Outlook, Excel and Power Point is required.Must be able to meet the physical demand of that this position including continuous lifting or moving from 5 to 25 pounds weight material.Availability to work all shifts as neededPreferred:* Knowledge of Food and Drug Administration (FDA), European Medicines Agency (EMA), and current Good Manufacturing Practices (cGMP) regulations is preferred.* Pharmaceutical/Good Manufacturing Practice (GMP) experience.* Proven experience leading a team in a manufacturing environment.Other:* Ability to be based in Fort Washington, PA and requires up to ten percent (10%) of travel.

　　Equal Opportunity Employer-minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity