Will also consider above experience from other highly regulated manufacturers/industries, e.g., Automotive, Defense/Aerospace, Consumer Electronics, Consumer Packaged Goods, or similar.Īt Abbott, you can have a good job that can grow into a great career.Experience with regulated medical device manufacturing.Manufacturing management experience in manufacturing planning, documented systems, GMP, and Quality.Experience with ISO 9001/CE Mark requirements.Experience in state-of-the-art, multi-step, high volume, process control manufacturing and process development.Proven leadership skills, results oriented, highly collaborative, team player, and self-starter who can operate in a fast-paced environment.Manufacturing experience with companies engaged in the manufacture of high quality, FDA regulated products.Knowledge of regulations and standards of medical devices.Minimum of 10 years related experience in the following: An equivalent combination of education and work experience.Being accountable for production of commercial and development builds.Participating in new product design and development reviews and design control activities effecting manufacturing.Advising and assisting the Director of Operations in general areas of manufacturing.Managing financial costs and look for cost effective solutions.Developing key performance indices, setting goals and developing plans for continuous improvement in quality, cost, employee performance, and maintaining a high level of employee safety.Being driven by and understanding schedules, quality, and costs.Being responsible for the activities to manufacture product to design requirements, FDA guidelines and operating procedures.Developing, establishing, and maintaining operational objectives and assignments.MANAGE AND EMPOWER A SIZABLE MANUFACTURING ORGANIZATION BY: Will manufacture product for clinical trials, experimental trials and saleable product. Identifies and executes continuous improvement opportunities. Selects and develops personnel to ensure the efficient operation of the production function. Plans and administers procedures and budgets, both operational and capital. The role will prioritize production schedules based on product introduction, equipment efficiency, and materials supply. This position is responsible for the development and implementation of manufacturing and process development activities to meet production schedules, quality standards, and cost objectives in a regulatory environment. Hours: Shift B (day) runs Monday – Friday starting at 1, 2 & 3 pm.Provide production leadership for semi-automatic manufacturing operations.Our location in GURNEE, IL currently has an opportunity for an OPERATIONS MANAGER.
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