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Bentec Medical Opco LLC is looking for an Extruder Operator in Woodland, California. The successful candidate will set up and operate machines for extruding silicone material in manufacturing OEM and medical products. A high school diploma and at least four years of experience are required.
The role involves duties such as installing machine parts, adjusting controls, measuring product specs, and ensuring product quality. Candidates must have strong technical skills and the ability to work with mathematical concepts.
Job Title: Extruder Operator
Department: Manufacturing
FLSA Status: Hourly Non-exempt
Sets up and operates machine to extrude silicone material for the manufacture of OEM and medical products by performing the following duties:
Duties include, but are not limited to the following, as other duties may be assigned.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Must have a high school education and at least four years of experience operating silicone extruders. Must know how to adjust temperature, pressures and speed of machinery.
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routing reports and correspondence. Ability to speak effectively before groups of customers or employees organization.
Ability to work with mathematical concepts such as probability and statistical inference; ability to apply concepts such as fractions, percentages, ratios and proportions to practical situations. Must be able to convert between standards, e.g., English to Metric conversion, liquid and solid measures, weight counting, etc.
Ability to define problems, collect data, establish facts and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
Working knowledge of cGMP (QSR)/ISO 13485:2006, EN46001 and Medical Device Directives. Knowledge of Microsoft Office computer programs and previous technical writing experience with clear written and verbal communication skills. Knowledge of MRP computer programs, understanding of statistical process control methods.