Verify employee’s time in KRONOS, Work with Supervisors in other departments to coordinate activities, University degree in Manufacturing, Chemistry, or Engineering (concentration in Food Industry is preferred), Has knowledge of manufacturing systems (SA, Mfg Pro), good PC literacy (MS Office), Must have 3 - 4 years experience in Manufacturing (Production, Maintenance, and Engineering preferred), Experience in managing / supervising team leaders / blue collar workers, Manage daily line operations in Mixing, Baking, and Packaging. Please enter your email address. Work is reviewed for soundness of judgement, overall adequacy and accuracy, (Supervision Provided) Provides direction and guidance to predominantly non-exempt and entry level exempt personnel; evaluates performance of and assists in career development planning for subordinates; often responsible for a local functional or process activity, Practical knowledge of pharmaceutical manufacturing processes, Knowledge of pharmaceutical standards and quality systems, Basic understanding of cGMP requirements (Indonesia/ASEAN), Monitors, organizes and performs all functions associated with packaging of clinical trial supplies and assures compliance to GMPs, SOPs, FDA, DEA and OSHA rules and regulations, Implements procedures to increase productivity and decrease downtime, Works closely with Project Management to establish manufacturing and packaging protocol section of batch record for ongoing and future studies, Oversees both primary and secondary production areas equipped with various pharmaceutical packaging equipment including but not limted to: automated bottle line, form, fill and seal equipment, card sealing, vial and ampoule labelers, pouch equipment and medical device tray sealing, Responsible for production involving manual and automated application of randomized labels on bottles, cards, cartons, kits, vials, syringes and ampoules, Responsible for insuring correct placement of multiple look-alike product combinations in blister units, cards and bottles, Employee performance evaluations, new employee hiring, disciplinary notices, employee termination, according to company guidelines and performance requirements as established in the union contact, Develops, reviews and edits related production SOP’s (operational, maintenance, cleaning) in Documentum program, Responsible for maintaining and ordering personnel, safety, disposable and support packaging supplies, Review and approval of production staff vacation and personal days, along with leave of absence requests, Responsible for entering data accurately in batch records and logbooks, Must review completed manufacturing and packaging batch records in a timely manner, Investigate and prepare out of specification reports and customer complaints related to production in Trackwise program, Responsible for handling the packaging of refrigerated and frozen clinical trial material, Security, accountability and reconciliation of controlled substance in clinical production, Staging, reconciliation and inventory label generation in ERP system (JD Edwards), Data entry required for production rates, labor hours and downtime, Responsible for daily employee assignment training, Bachelor of Science Degree in Health/Chemistry/Pharmacy related field is preferred, Clinical Trial Manufacturing and Packaging experience is preferred, Completed Clinical Trial training course is preferred, Computer literate (Microsoft Suite, Word, Outlook, etc) is required, JD Edwards experience or similar ERP systems experience is required, Working knowledge of cGMPs, DEA and OSHA rules and regulations is required, Leadership and team building skills are preferred, Demonstrate ability to train, motivate, direct and supervise production personnel are required, Knowledge of packaging equipment in a Just-in-Time environment is required, Proven ability to develop Standard Operating Procedures is preferred, This is Second Shift, 4:00 pm to 12:30 am. Develops and coaches employees using Cargill’s Performance Management Process (PMP) as well as managing the disciplinary process, 25% Operational Efficiency: Drives customer solutions and services, product quality, quality notifications, and food safety. How much does a Production Supervisor III make in the United States? Maxine can change manufacturing processes to make them more productive. You will monitor operations in conjunction with the EHS Coordinator assuring that we are following all safety and environmental regulations and specifications, Drive plant continuous improvement efforts and lean concepts with team. This production supervisor resume sample job description is for an individual with experience in the manufacturing industry. I have one year of experience = I have one year’s experience. Communicate hazards to others to prevent repeat incidents and raise the issue with maintenance or management. (Quality), Working knowledge of MS office products. La Mouche Production est une production indépendante qui propose des diffusions de spectacles vivants, des événementiels et du management d’artistes. Perform defined in process inspection, Task allocation-ensure that welders and metal worker know what to do, how to do and how long they need to complete specific tasks-in strict accordance to drawing and documentation requirements, Implement & Smoothly followed takt time on line and highlight takt time disturbances in time. Actively working to eliminate hazards that may cause injury. Adhering to company safety standards as they relate to daily operations, Responsible for the production, quality, and performance of the employees, Evaluates employees based on performance set forth in the evaluation guidelines and completes the require documentation, Recommends candidates for hire, promotion, demotion, transfer, or release, Responsible for maintaining labor within an assigned department levels, Reassigns labor on idle equipment to eliminate unfavorable labor variance. wrong; I am a production supervisor of the highest quality at a chemical … Contribute to continuous improvements in all areas of production, Ensure that production is efficient and effective with high level of employee engagement, Actively participate in day to day leadership of the business unit, and positively contribute to the business unit team, driving engagement activities, Lead / participate in continuous improvement activities, e.g. Grâce à ce paragraphe, vous pouvez contextualiser votre poste actuel. 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