Fabrication supervisor- med device - united states, irvine

We have an incredible client in irvine seeking a fabrication supervisor (must have medical device experience) and that can pay up to 85k.
schedule: 6:00 am - 2:30 pm

the supervisor is responsible for all the activities of production personnel engaged in all facets of the manufacturing functions. assumes authority for personnel actions and oversees the day-to-day operations to a group of professionals or skilled operational and technical employees including the initiation, flow, and completion of production jobs. relies on extensive experience and judgment to plan and accomplish goals and assist the management in the manufacturing operations, including final labeling and packaging, quality inspection and component stockroom activities. this position will work closely with production planning, quality, and other operations personnel to support the manufacturing operations. contributes to the performance management of employees and addresses issues pertaining to training, hiring, and terminating.

job responsibilities:hire, train, develop and supervise a team of production assemblers to achieve production plan.ensure the appliance is produced to quality specifications and standards.maintain inventory management and replenishment system for common components and packaging materials.attend and contribute to regularly scheduled production and planning meetings.oversee production lines to ensure a steady flow of product and attainment of the production schedule.oversee completion of all applicable documentation and logs as required. ensure good manufacturing practices are followed.comply with work rules including those pertaining to safety, environment and quality system.support the development, improvement, and maintenance of new and existing manufacturing processes.perform qualifications and assist in the execution of validations for manufacturing.represent area in all internal and external audits.participate in mrb and ensure all transactions and dispositions are handled promptlyresponsible for conducting performance reviews.implement and maintain quality inspection procedures.ensure appropriate level of trained personnel to complete production and inspection schedule and effective employee utilization.assist in collecting and providing key performance indicators (kpi's).troubleshooting processes and procedures resulting from the training that is not effective.contributes to the completion of cross-organizational projects and goals.engages in continuous-improvement objectives and seeks opportunities to support company growth.skills and qualifications:associate degree from an accredited institution with a minimum of four (4) years' experience in a cgmp environment, preferably in a medical device industry.experience as a subject matter expert (sme) in manufacturing systems, methods and procedures.strong ability to communicate orally and in writing.strong ability to influence in a team environment and collaborate with peers.demonstrated mathematical skills, including the ability to perform addition, subtraction, multiplication, division, and conversions.must demonstrate strong team management and participation skills and a thorough working knowledge of 21 cfr parts 820 (qsr) and iso 13485.demonstrated ability to read, comprehend, and follow written instructions.demonstrated written and verbal communication skills are required.must be able to perform computer operations such as ms office and outlook and other computer-based softwaredetail-oriented, and ability to work with cross-functional teams.demonstrated independent work initiative, sound judgment, diplomacy, analytical ability, and professional demeanor.physical demands/surroundings:an employee may be required to use protective clothing and gear such as gowns, shoe covers, hair covers, eye protection, and gloves as directed.lifting and carrying

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