International Vitamin Corporation (IVC) is a leading global manufacturer of vitamins and nutritional supplements with more than half a century of private label and contract manufacturing experience, an impeccable quality and regulatory compliance record, and with new resources focused on enriching the health and lives of others.
Responsible for maintaining GMP quality standards, plant safety and manufacturing productivity through-out Cell 1 department. In-depth knowledge and understanding of equipment to support set-ups, adjustments, repairs, and maintaining all granulation and continuous blending equipment in accordance with diagrams, sketches, operation manuals, and manufacturer's specifications. Performs routine set up on loss in weight feeders, formulations and monitors electronic logbooks transactions as required. Direct reports include all on-shift operators in Cell 1.
Monitors operators and equipment throughout shift to ensure all SOPs are properly followed and executed. Coaches operators on proper operation and addresses violations with proper documentation.Directs machine operators and service personnel in details of daily schedule, standard operating procedures and requirements.Ensures production schedule is maintained by making necessary corrections and adjustments to equipment to maintain maximum performance. Reports issues that may result in schedule not being maintained to management immediately.Adjusts process parameters and makes changes by setting up assigned equipment for change in material, size, and product. Tests equipment for quality of operation when changeover is completed.Routinely checks product for defects and imperfections. Examines finished product for conformity with quality specifications and records. Trains and supervises machine operators in their essential duties and safety precautions required when working on the equipment.Ensures accurate and timely completion of all equipment logs and documentation.Ensures proper cleanliness and assembly of all manufacturing equipment per the approved SOP.Responsible for maintaining a neat, clean and safe working environment at all times.Understands and adheres to all cGMP and FDA regulations.Identifies and reports any quality issues to management or quality department.Understands and adheres to all Company policies, procedures, SOPs and Safety regulations.Other duties as assigned
Experience in GMP environment (Preferably in Pharmaceutical Industry)Team building skills and leadership qualitiesAbility to read, write, and communicate in English.Ability to understand basic math.Ability to follow SOPs and cGMPs, i.e., wearing appropriate clothing, beard covers, gloves, etc.Basic computer knowledge.Must maintain a positive attitude and a willingness to learn and develop skills.Ability to interact with other department Technicians, Schedulers, Product development and Information Services.The ability to work independently, within a production team and without supervision.Willingness to work overtime when needed.Develop and Coach operators as needed.IVC is proud to be an Equal Opportunity Employer M/F/D/V EOEWorking ConditionsAbility to work Mandatory Overtime (Weekends) and Shift Work with required noticePhysical RequirementsJob requires the ability to stand for long periods of timeRequires the ability to lift 50 lbs.Perform repetitive tasksAbility to operate a forklift or pallet jack
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Are you ready to take on an exciting challenge as the Lead, Granulation at International Vitamin Corporation (IVC) in Greenville? In this pivotal role, you will be responsible for maintaining GMP quality standards while ensuring plant safety and improving manufacturing productivity within the Cell 1 department. You’ll be working hands-on with granulation and continuous blending equipment, applying your expertise to set up, adjust, and repair machinery in alignment with operation manuals and specifications. Your keen eye for detail will be essential as you monitor operators and equipment during shifts, ensuring that all standard operating procedures (SOPs) are executed flawlessly. Not only will you lead a team of on-shift operators, but you'll also be coaching them on best practices and addressing any violations promptly. Collaboration is key in this role, so you’ll interact with other departments to maintain the production schedule and quickly report any potential issues to management. Quality is at the heart of what we do at IVC, and you will be responsible for checking the finished product for specifications and defects, maintaining accurate logs, and ensuring a clean and safe working environment. If you have a background in a GMP environment, a passion for team building, and a proactive attitude, this is the perfect opportunity to showcase your leadership skills and contribute significantly to our mission of enriching lives through nutritional excellence!
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